Medical specialty
Genetics Testing in Dubai & UAE
A clear, patient-friendly guide to Genetics diagnostics — what these investigations look for, how samples are collected, and what to expect from your report.
- Quality-controlled laboratory
- Home collection across the UAE
- Confidential handling of results
Clinical overview
About Genetics
Testing areas
Explore Genetics testing areas
Choose a testing area below to see the investigations it covers — specimen type, turnaround time and listed prices. All prices are confirmed with you before any sample is collected.
274 testing areas
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Next-Generation Sequencing
7 testsNavigating complex, undiagnosed health challenges requires the most advanced genetic insights available to illuminate the bes...
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NGS
1 testWhen standard genetic testing leaves questions unanswered, delving deeper into your genomic blueprint brings profound, empowe...
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NGS Genetic
9 testsUnderstanding your underlying genetic predispositions empowers you and your family to make proactive, highly informed decisio...
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NGS Panel
1 testInvestigating specific clinical symptoms like neurodevelopmental delays or hereditary cancer risks demands a targeted, high-r...
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NGS Sequencing
1 testAchieving a definitive diagnosis for complex, multi-system disorders requires the highest level of genetic analysis to provid...
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NGS Single Gene
2 testsWhen clinical symptoms strongly point toward a specific inherited condition, highly focused genetic testing provides the exac...
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Obesity Genetics
2 testsStruggling with severe or early-onset weight management challenges can be deeply frustrating, but uncovering the underlying g...
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Oculocutaneous Albinism
1 testNavigating an unexpected diagnosis of skin and vision pigmentation changes requires compassionate, highly precise genetic ins...
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Ophthalmic Genetic
3 testsExperiencing unexplained vision loss or inherited eye conditions can be alarming, but securing exact genetic answers offers a...
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Ophthalmic Genetics
5 testsUnderstanding the hereditary risks affecting your family’s eye health empowers you to make proactive, highly informed decisio...
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Ophthalmology Genetic
2 testsExperiencing unexplained vision changes or navigating a family history of eye disease can be alarming, but securing exact gen...
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Ophthalmology Genetic Panel
1 testDiagnosing complex, overlapping visual symptoms requires a comprehensive approach to ensure no crucial detail is missed. With...
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Ophthalmology Genetics
7 testsSafeguarding your family’s ocular health starts with a deep understanding of your hereditary blueprint, giving you the power...
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Osteogenesis Imperfecta
7 testsDealing with frequent, unexplained bone fractures in yourself or a child is incredibly distressing, but finding the exact bio...
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Osteopetrosis Genetic
1 testInvestigating atypical, overly dense bones requires highly specialized diagnostics to uncover the rare metabolic roadblocks a...
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Osteoporosis Genetics
1 testA strong family history of severe bone density loss warrants proactive, empowering insights before fractures occur, allowing...
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Parkinson Disease Genetic
3 testsNavigating early-onset motor symptoms or a family history of movement disorders can be deeply unsettling, but uncovering the...
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Parkinson Disease Genetics
3 testsUnderstanding the broader hereditary factors behind neurodegenerative conditions empowers families to plan for the future wit...
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Peroxisomal Disorders
2 testsConfronting complex neurological and metabolic symptoms in a newborn or young child demands urgent, precise clarity to ensure...
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Pharmacogenomics
14 testsEnduring the trial-and-error process of finding the right medication can be exhausting and dangerous, but precision medicine...
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Platelet Disorders
3 testsExperiencing unexplained bruising, prolonged bleeding, or abnormal clotting can be deeply unsettling, but securing precise ge...
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Polycystic Kidney Disease
2 testsA family history of kidney issues or the sudden onset of hypertension and renal cysts warrants proactive, empowering insights...
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Pompe Disease
1 testConfronting unexplained muscle weakness or respiratory difficulties in a newborn or adult demands urgent, highly specific dia...
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Pontocerebellar Hypoplasia
1 testNavigating severe developmental delays or neurological symptoms in a newborn is incredibly overwhelming, but finding the exac...
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Porphyria Genetic
1 testEnduring sudden, severe abdominal pain, extreme sun sensitivity, or unexplained neurological symptoms can be exhausting, but...
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Prader-Willi Syndrome
3 testsConcerns regarding neonatal low muscle tone, developmental delays, or relentless childhood appetite require compassionate, hi...
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Preimplantation Genetic Diagnosis
3 testsBuilding a family while navigating known hereditary genetic risks can be emotionally complex, but advanced science offers pro...
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Prenatal
4 testsAnticipating a new baby is a joyous milestone, and proactively securing insights into their health provides the ultimate reas...
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Prenatal Chromosomal Analysis
1 testNavigating high-risk pregnancy factors or abnormal ultrasound findings demands the highest level of precise, specialized diag...
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Prenatal Chromosome Analysis
1 testConfirming the microscopic structural integrity of your baby's DNA brings unparalleled clarity and reassurance during complex...
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Prenatal Cytogenetics
2 testsInvestigating potential fetal anomalies requires highly precise microscopic analysis to ensure you receive the definitive rea...
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Prenatal Genetic
3 testsPreparing for a healthy baby starts with understanding your unique hereditary blueprint, empowering expectant parents with pr...
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Primary Ciliary Dyskinesia
14 testsEnduring chronic, unexplained respiratory infections or persistent sinus issues from childhood can be exhausting, but finding...
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Primary Immunodeficiency
14 testsCoping with unusually frequent, severe, or hard-to-treat infections demands a deep dive into your body’s foundational defense...
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Acute Promyelocytic Leukemia
1 testFacing a sudden, aggressive leukemia diagnosis requires immediate, highly specific genetic insights to unlock the most effect...
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Progeria
1 testConfronting the signs of accelerated aging or unusual developmental delays in a young child requires compassionate, highly pr...
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Adrenal Disorders
1 testUnexplained imbalances in stress hormones, blood pressure, or physical development often trace back to hidden hereditary fact...
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Pseudohypoaldosteronism
1 testDealing with dangerous sodium loss, severe dehydration, or electrolyte imbalances in a newborn or infant demands rapid, highl...
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Adrenoleukodystrophy
1 testNavigating progressive neurological changes or unexplained adrenal insufficiency in a child or adult requires incredibly prec...
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Psoriasis Genetics
1 testStruggling with severe, persistent psoriasis or an early-onset autoimmune condition can be frustrating, but uncovering your u...
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AIMP1 Gene
1 testConfronting severe neurodevelopmental delays or hypomyelinating leukodystrophy in a young child demands the highest level of...
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Rare Genetic Disorders
1 testSearching for answers to complex, unexplained, or multi-system symptoms can be an exhausting diagnostic journey, but advanced...
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Albinism
1 testAddressing unexpected skin, hair, and eye pigmentation changes requires compassionate, precise genetic insights to optimize l...
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Red Cell Enzyme Defects
1 testEnduring unexplained episodes of hemolytic anemia, jaundice, or chronic fatigue demands a deep look into the microscopic meta...
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Albinism Genetic
3 testsUnderstanding the exact hereditary pathways of albinism in your family empowers you to make proactive, highly informed decisi...
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Renal Genetic
1 testA family history of progressive kidney disease or the early onset of unexplained renal symptoms warrants proactive, empowerin...
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Alport Syndrome
2 testsManaging a family history of kidney disease accompanied by hearing loss or vision changes demands highly specific diagnostic...
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Reproductive Genetics
8 testsPlanning for a healthy family starts with a deep understanding of your unique hereditary blueprint, giving expectant parents...
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ALS Genetic
5 testsFacing a family history of progressive muscle weakness or motor neuron decline is incredibly daunting, but securing precise g...
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Retinal Disorders
1 testExperiencing unexplained vision changes or progressive vision loss can be deeply alarming, but securing exact genetic answers...
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Alzheimer's Disease Genetics
1 testA family history of early cognitive decline or memory loss understandably causes anxiety, but understanding your personal gen...
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Retinal Dystrophy Genetics
1 testUnderstanding the hereditary factors behind progressive retinal issues empowers you to make proactive, highly informed decisi...
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Amelogenesis Imperfecta
1 testDealing with severe, unexplained tooth discoloration, extreme sensitivity, or rapid enamel wear requires specialized diagnost...
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Rett Syndrome
5 testsNavigating severe developmental regression or unexplained neurological symptoms in a young child demands immediate, precise d...
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Rheumatoid Arthritis Genetic
1 testA strong family history of chronic joint pain or autoimmune inflammation warrants proactive insights before severe symptoms p...
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Amyotrophic Lateral Sclerosis Genetic
1 testUnderstanding the specific genetic drivers behind progressive motor neuron disease empowers patients and families to make hig...
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Sequencing
19 testsAchieving a definitive diagnosis for complex, multi-system symptoms requires the most comprehensive look at your fundamental...
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Androgen Receptor Disorders
1 testNavigating unexpected physical development, atypical puberty, or unexplained fertility challenges requires deeply precise end...
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Single Gene
332 testsWhen clinical symptoms or family history point directly toward a specific inherited condition, highly focused genetic testing...
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Aneuploidy
1 testWhether investigating unexplained pregnancy loss or seeking reassurance regarding your child's developmental health, definiti...
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Single Gene Analysis
26 testsSecuring precise diagnostic confirmation for a suspected hereditary condition demands a deeply focused, high-resolution analy...
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Aortopathy
1 testA family history of sudden aortic aneurysms or dissections warrants urgent, proactive insights to protect your cardiovascular...
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Single Gene Disease
1 testConfronting the possibility of a targeted hereditary condition requires highly precise diagnostics to unlock the right specia...
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Aromatase Deficiency
1 testDealing with atypical skeletal growth, delayed puberty, or complex hormonal imbalances demands highly specific diagnostic car...
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Single Gene Disorder
72 testsFinding the exact biological cause of a suspected genetic condition brings empowering clarity and a clear path to targeted re...
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Arrhythmogenic Cardiomyopathy
1 testConfronting unexplained heart palpitations, fainting spells, or a family history of sudden cardiac events requires the highes...
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Single Gene Disorders
133 testsUnderstanding your family's risk for specific hereditary conditions empowers you to make proactive, highly informed health an...
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Arthrogryposis Genetic
1 testCoping with a child’s congenital joint contractures can be overwhelming, but uncovering the precise biological root provides...
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Single Gene Mutation
1 testWhen a specific hereditary condition runs in your family, getting precise confirmation can alleviate anxiety and provide a cl...
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Ataxia Genetic
3 testsDealing with a progressive loss of balance, coordination, or speech can be deeply unsettling, but securing precise genetic an...
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Single Gene Mutation Analysis
4 testsSecuring precise diagnostic confirmation for a suspected genetic trait demands a deeply focused, high-resolution analytical a...
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Ataxia Panels
1 testWhen neurological symptoms overlap and point to multiple potential movement disorders, an expansive, high-resolution diagnost...
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Single Gene Mutations
1 testUnderstanding your underlying genetic predispositions empowers you and your family to make proactive, highly informed health...
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Autism Genetic
4 testsSearching for answers regarding a child's unique neurodevelopmental path can be an emotional journey, but targeted molecular...
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Single Gene Sequencing
297 testsAchieving a definitive diagnosis for a monogenic disorder often requires reading the entire genetic code of a specific gene t...
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Autism Genetics
5 testsUnderstanding the broader hereditary factors associated with neurodevelopmental differences empowers families to access the m...
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Skeletal Disorders
1 testNavigating unexplained bone fragility, frequent fractures, or structural anomalies requires highly specialized diagnostic car...
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Autism Spectrum Disorder
1 testSeeking answers for a child's unique social, communication, or behavioral development can be an emotional journey, but target...
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Skeletal Dysplasia
3 testsConcerns regarding a child’s disproportionate growth, short stature, or bone development demand compassionate, highly precise...
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Autism Susceptibility
1 testUnderstanding the hereditary factors associated with neurodevelopmental nuances empowers families to access the most effectiv...
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Skeletal Dysplasia Sequencing
1 testWhen standard clinical evaluations leave questions about complex bone development unanswered, advanced genomic science brings...
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Autoimmune Disorders
1 testDealing with chronic inflammation, joint pain, or unexplained systemic symptoms often points to a misguided immune system, an...
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Spinocerebellar Ataxia
14 testsConfronting progressive loss of coordination, balance issues, or a family history of movement disorders can be deeply unsettl...
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Autoimmune Lymphoproliferative Syndrome
2 testsConfronting chronic swollen lymph nodes, an enlarged spleen, or unexplained blood cytopenias requires incredibly specific dia...
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Thalassemia
10 testsA family history of chronic anemia or unexplained fatigue warrants proactive, empowering insights to protect your health and...
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Autoinflammatory Disorders
1 testEnduring recurrent, unexplained fevers, severe joint pain, or persistent skin rashes from childhood can be exhausting, but fi...
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Thalassemia Mutation Analysis
1 testDealing with a diagnosed hemoglobin disorder requires highly specific diagnostic clarity to unlock the safest, most effective...
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Bardet-Biedl Syndrome
4 testsConfronting complex, overlapping symptoms such as early-onset vision loss, obesity, or developmental delays in a child demand...
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Thyroid Disorders
1 testUnexplained metabolic shifts, persistent fatigue, or a strong family history of thyroid issues can be concerning, but uncover...
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Beckwith-Wiedemann Syndrome
1 testNavigating concerns about a child's disproportionate growth, asymmetrical physical features, or neonatal hypoglycemia require...
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Treacher Collins Syndrome
1 testNavigating congenital craniofacial differences in a newborn requires highly specialized, compassionate diagnostic care to ens...
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Brugada Syndrome
3 testsA history of unexplained fainting, irregular heartbeats, or sudden cardiac events in your family requires immediate, highly f...
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Vascular Genetic Disorders
2 testsA family history of sudden aortic aneurysms or unexplained vascular events warrants proactive, life-saving insights to protec...
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Cancer Genetic
1 testUnderstanding your personal susceptibility to hereditary malignancies transforms anxiety into empowering, proactive control o...
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Waardenburg Syndrome
1 testAddressing unexpected hearing loss accompanied by unique pigmentation changes in a child demands precise diagnostic answers t...
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Cancer Genetics
59 testsEmpowering yourself with a deep understanding of your family’s oncological history is the most effective way to protect your...
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WHIM Syndrome
1 testCoping with chronic neutropenia, unusually frequent infections, or persistent warts requires incredibly specific immunologica...
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Cancer Panel
5 testsUnderstanding your hereditary risk for multiple cancers allows you to take decisive, life-saving preventative action before s...
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X-linked Disorders
1 testUnderstanding how specific conditions are inherited through your family line is a crucial, empowering step toward protecting...
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Cardiac Genetics
4 testsA family history of sudden heart issues or unexplained cardiovascular symptoms warrants proactive insights to protect your li...
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X-linked Mental Retardation
1 testSeeking answers for a child's unexplained developmental delays or intellectual challenges can be an emotional journey, but de...
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Cardiomyopathy Genetic
40 testsNavigating unexplained heart failure or an enlarged heart requires highly specific diagnostic clarity to unlock the most effe...
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Xeroderma Pigmentosum
2 testsExtreme sensitivity to sunlight and an early risk of severe skin changes demand urgent, precise diagnostic clarity to establi...
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Cardiomyopathy Genetics
7 testsUnderstanding the broader hereditary factors affecting your heart's structural integrity empowers your family to make proacti...
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Cardiomyopathy Panel
2 testsWhen cardiac symptoms point toward an inherited structural issue, an expansive, high-resolution diagnostic approach is essent...
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Cardiovascular Genetic
7 testsProtecting your heart means looking beyond standard lipid tests to uncover the precise molecular blueprint governing your car...
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Cardiovascular Genetics
39 testsA family history of sudden heart issues or unexplained cardiovascular symptoms warrants proactive insights to protect your li...
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Carrier Screening
2 testsPlanning for a healthy family starts with a deep understanding of your unique hereditary blueprint, giving expectant parents...
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Cataract Genetic
1 testExperiencing early-onset clouding of the eye lens or navigating a family history of childhood cataracts demands precise diagn...
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Charcot-Marie-Tooth Disease
10 testsCoping with progressive muscle weakness, loss of sensation in the limbs, or high foot arches can be deeply unsettling, but se...
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Charcot-Marie-Tooth Type 4A
1 testNavigating severe, early-onset peripheral neuropathy requires incredibly specific diagnostic clarity to unlock the safest, mo...
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Cholestasis Genetics
1 testEnduring severe itching, unexplained jaundice, or elevated liver enzymes demands a deep molecular look into your liver's bile...
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Chromosomal Abnormalities
1 testWhether investigating developmental delays, multiple miscarriages, or congenital anomalies, identifying the underlying struct...
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Chromosomal Analysis
3 testsAchieving a complete, microscopic understanding of your genetic architecture is a vital step when diagnosing complex reproduc...
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Chromosomal Karyotyping
1 testNavigating high-risk pregnancy factors, infertility, or ambiguous physical development requires the highest level of proven,...
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Chromosomal Microarray
9 testsWhen a child presents with unexplained autism, developmental delays, or congenital anomalies, a standard chromosomal test may...
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Chronic Granulomatous Disease
3 testsEnduring unusually severe, recurrent bacterial or fungal infections from a young age demands a deep dive into the microscopic...
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CMT Genetic
2 testsCoping with progressive muscle weakness, numbness in the extremities, or distinct high foot arches can be deeply unsettling,...
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Coagulation Disorders
13 testsA family history of severe, unexplained bleeding episodes or recurrent, dangerous blood clots requires proactive molecular in...
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Complement Deficiency
1 testDealing with recurrent severe infections or the early onset of complex autoimmune conditions like lupus requires a deep inves...
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Cone-Rod Dystrophy
1 testExperiencing a progressive loss of color vision, extreme light sensitivity, or a steady decline in visual sharpness can be al...
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Congenital Adrenal Hyperplasia
1 testNavigating unexplained hormonal imbalances, atypical physical development, or severe salt-wasting crises in a newborn demands...
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Congenital Glycosylation Disorders
1 testSearching for answers regarding a child's unexplained developmental delays, low muscle tone, or multi-organ dysfunction can b...
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Congenital Myasthenia
1 testConfronting profound muscle weakness, severe fatigue, or drooping eyelids that are present from birth requires incredibly pre...
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Connective Tissue Disorders
2 testsCoping with extreme joint hypermobility, unexpected vascular issues, or severe skin fragility warrants proactive, overarching...
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Corneal Dystrophy
2 testsExperiencing progressive clouding of the eye, severe glare, or recurrent corneal erosions demands specialized diagnostic clar...
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Craniosynostosis
3 testsAddressing an abnormal head shape or restricted skull growth in an infant requires deeply compassionate, highly precise diagn...
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Cystinosis
1 testDealing with early-onset kidney dysfunction, extreme thirst, or the buildup of crystalline deposits in the eyes requires high...
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Cytogenetics
30 testsAchieving a comprehensive understanding of your foundational chromosomal architecture is essential when navigating complex re...
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Cytogenetics and FISH
1 testNavigating a complex hematological cancer or a suspected congenital disorder requires a multi-layered diagnostic approach to...
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Deafness
1 testDiscovering unexpected hearing loss in a newborn or experiencing progressive auditory decline can be deeply emotional, but fi...
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Deafness Genetic
9 testsWhen a family history of hearing loss points toward a specific hereditary trait, getting precise molecular confirmation is cr...
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Deafness Genetics
11 testsUnderstanding the broader hereditary landscape of auditory health empowers you to make fully informed, proactive decisions fo...
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Dementia Genetic
2 testsA family history of early-onset cognitive decline or severe memory loss is understandably frightening, but unlocking your per...
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Dermatologic Genetic
1 testDealing with severe, unexplained skin blistering, extreme scaling, or pigment loss requires specialized diagnostic insights t...
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DGKE Gene Analysis
1 testNavigating severe, early-onset kidney dysfunction or a suspected case of atypical hemolytic uremic syndrome (aHUS) demands ra...
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Diabetes Genetic
2 testsWhen diabetes strikes unusually early in life or doesn't fit the typical Type 1 or Type 2 profiles, uncovering the exact mole...
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Diamond-Blackfan Anemia
5 testsConfronting severe anemia in a newborn or infant requires highly specialized diagnostic clarity to distinguish an inherited b...
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DNA Profiling
2 testsWhether seeking definitive proof of biological relationships, resolving immigration requirements, or securing personal identi...
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Dyskeratosis Congenita
1 testEnduring unexplained bone marrow failure, abnormal nail growth, or distinct skin pigmentation changes demands a deep look int...
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Ehlers-Danlos Syndrome
7 testsCoping with extreme joint hypermobility, fragile skin, or unexplained chronic pain requires proactive, overarching insights t...
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Endocrine Genetic
2 testsUnexplained hormonal imbalances, sudden metabolic shifts, or atypical physical development often trace back to hidden heredit...
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Endocrine Genetic Disorders
1 testA family history of complex glandular tumors or widespread hormonal issues warrants proactive, expansive insights to protect...
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Epidermolysis Bullosa
2 testsAddressing the presence of extremely fragile, easily blistering skin in a newborn or infant requires deeply compassionate, hi...
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Epilepsy Genetic
2 testsDealing with the sudden onset of childhood seizures or treatment-resistant epilepsy can be an exhausting diagnostic journey,...
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Epilepsy Genetics
10 testsUnderstanding the broader hereditary factors associated with seizure disorders empowers families to access the most effective...
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Erythrocytosis Genetic
2 testsAn unexplained, dangerous overproduction of red blood cells requires highly specific diagnostic insights to prevent severe ca...
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Familial Adenomatous Polyposis
1 testA family history of countless colon polyps or early-onset colorectal cancer warrants urgent, proactive molecular insights to...
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Familial Aortic Aneurysm
1 testNavigating a family history of sudden, silent vascular emergencies like thoracic aortic dissections demands the highest level...
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Familial Hypercholesterolemia Genetic
1 testStruggling with dangerously high cholesterol that doesn't respond to diet or exercise is often a sign of a hidden hereditary...
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Fanconi Anemia
8 testsDealing with unexplained severe bone marrow failure, unusual physical abnormalities, or an extreme predisposition to early ca...
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Fanconi Anemia Genetic
2 testsWhen standard cellular breakage tests suggest Fanconi Anemia, pinpointing the exact genetic mutation is essential for unlocki...
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FISH Analysis
2 testsInvestigating elusive, sub-microscopic chromosomal deletions or precisely classifying a malignant tumor requires the highest...
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FMR1-Related Disorders
1 testNavigating a family history of intellectual disabilities, unexplained premature ovarian failure, or late-onset tremors requir...
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Fragile X Syndrome
3 testsAddressing a child's developmental delays, autism spectrum behaviors, or learning challenges demands compassionate, highly sp...
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Gene Mutation Analysis
6 testsWhen clinical symptoms point strongly toward a specific hereditary condition, getting a precise, targeted confirmation is ess...
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Gene Sequencing
143 testsAchieving a definitive diagnosis for a complex or rare genetic disorder often requires reading the entire genetic code of spe...
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Genetic Deafness
4 testsDiscovering unexpected hearing loss in a newborn or experiencing progressive auditory decline requires finding the exact biol...
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Genetic Disease
23 testsConfronting the possibility of a hereditary illness requires highly precise diagnostics to unlock the right specialized care...
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Genetic Disorders
136 testsUnderstanding your family's risk for specific hereditary conditions empowers you to make proactive, highly informed health an...
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Genetic Eye Disorders
3 testsExperiencing unexplained vision changes or navigating a family history of childhood blindness can be alarming, but securing e...
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Genetic for Ataxia
1 testDealing with a progressive loss of balance, coordination, or speech is deeply unsettling, but precise genetic confirmation of...
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Genetic for Hermansky-Pudlak Syndrome
1 testNavigating a complex presentation of albinism combined with unexpected bleeding issues or respiratory concerns requires incre...
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Genetic for Inherited Disorders
2 testsA family history of chronic illness or unexplained generational symptoms warrants proactive, empowering insights to break the...
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Genetic for Metabolic Disorders
4 testsAddressing sudden metabolic crises, unexplained developmental delays, or severe lethargy in a newborn demands rapid, highly s...
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Genetic Hearing Loss
8 testsWhen a family history of deafness points toward a specific hereditary trait, getting precise molecular confirmation is crucia...
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Genetic Hematology
2 testsInvestigating chronic anemias, abnormal clotting, or complex blood disorders requires a deep look into the inherited molecula...
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Genetic Immunodeficiency
1 testEnduring unusually severe, hard-to-treat infections from childhood demands a deep dive into the foundational defense mechanis...
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Genetic Myopathy
1 testCoping with unexplained muscle weakness, severe cramping, or delayed motor milestones in a child requires highly specific dia...
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Genetic Neurological Disorders
5 testsNavigating a family history of progressive movement disorders, early cognitive decline, or severe neuropathies warrants proac...
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Genetic Panel
7 testsInvestigating complex, overlapping clinical symptoms demands a targeted, high-resolution diagnostic approach to ensure no cru...
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Genetic Panels
15 testsWhen clinical symptoms are ambiguous and point to multiple potential conditions, having access to a specialized suite of targ...
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Genetic Screening
4 testsSafeguarding your future and your family's health begins with proactive, empowering insights that bring unparalleled reassura...
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Genetic Sequencing
256 testsAchieving a definitive diagnosis for multi-system or exceptionally rare disorders requires reading the deepest layers of your...
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Genetic Syndromes
13 testsNavigating a complex presentation of overlapping physical, developmental, and intellectual symptoms in a child demands highly...
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Glaucoma Genetic
1 testA family history of early-onset vision loss or severely elevated eye pressure warrants urgent, proactive insights to preserve...
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Glycogen Storage Disease
3 testsNavigating unexplained episodes of severe low blood sugar, profound muscle weakness, or an enlarged liver in a child demands...
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Hearing Loss
6 testsDiscovering unexpected auditory decline or diagnosing congenital deafness in a newborn can be deeply emotional, but pinpointi...
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Hearing Loss Genetic
5 testsWhen a family history of deafness points toward a specific hereditary trait, getting precise molecular confirmation is crucia...
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Hearing Loss Genetics
20 testsUnderstanding the broader hereditary landscape of auditory health empowers you to make fully informed, proactive decisions fo...
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Heart-Hand Syndrome
1 testConfronting overlapping congenital anomalies involving both the upper limbs and the cardiovascular system requires incredibly...
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Hematologic Genetic
1 testManaging a family history of overlapping blood disorders warrants proactive, expansive insights to protect your long-term vas...
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Hematologic Genetics
1 testManaging a family history of overlapping blood disorders warrants proactive, expansive insights to protect your long-term vas...
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Hemoglobinopathies
6 testsDealing with severe fatigue, chronic anemia, or sudden pain crises requires highly rigorous diagnostic oversight to identify...
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Hemoglobinopathy Genetics
1 testWhen standard blood tests suggest a specific inherited hemoglobin disorder, pinpointing the exact genetic mutation is essenti...
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Hemophagocytic Lymphohistiocytosis
4 testsNavigating sudden, overwhelming systemic inflammation, a dangerously enlarged spleen, and persistent high fevers in a child o...
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Hemophilia
1 testExperiencing severe, prolonged bleeding after minor injuries or suffering from painful, spontaneous joint bleeds requires pro...
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Hemophilia A
3 testsWhen clinical symptoms point specifically toward a Factor VIII deficiency, getting a targeted, high-resolution genetic confir...
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Hereditary Cancer
16 testsUnderstanding your personal susceptibility to familial malignancies transforms anxiety into empowering, proactive control ove...
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Hereditary Cancer Syndromes
2 testsEmpowering yourself with a deep understanding of your family’s complex oncological history is the most effective way to prote...
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Hereditary Cholestasis
1 testDealing with severe, chronic itching, progressive jaundice, or unexplained liver damage demands a deep molecular look into yo...
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Hereditary Deafness
3 testsAddressing a family history of profound hearing loss or navigating unexpected auditory challenges in a newborn requires compa...
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Hereditary Disorders
3 testsA family history of chronic illnesses or overlapping, unexplained generational symptoms warrants proactive, empowering insigh...
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Hereditary Eye Disorders
1 testExperiencing progressive vision changes, extreme light sensitivity, or navigating a family history of childhood blindness can...
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Hereditary Hair Disorders
1 testDealing with severe, unexplained hair loss from childhood or structural abnormalities that cause the hair shaft to break easi...
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Hereditary Hearing Loss
8 testsUnderstanding the precise genetic factors behind progressive or congenital auditory decline empowers you to make fully inform...
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Hereditary Hemorrhagic Telangiectasia
2 testsConfronting severe, recurrent nosebleeds, unexplained anemia, or the sudden discovery of vascular malformations in your lungs...
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Hereditary Multiple Exostoses
1 testNavigating unexpected bone bumps, restricted joint movement, or chronic pain in a growing child demands highly precise diagno...
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Hereditary Neuropathy
2 testsCoping with progressive muscle weakness, persistent numbness in the hands and feet, or distinct structural changes like high...
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Hereditary Ovalocytosis
1 testWhen standard blood smears reveal uniquely oval-shaped red blood cells, confirming the underlying genetic cause is essential...
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Hereditary Spastic Paraplegia
4 testsDealing with the gradual onset of severe leg stiffness, progressive muscle weakness, and spasticity can be an exhausting diag...
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Hirschsprung Disease
1 testDealing with a newborn's severe intestinal blockages or chronic, life-threatening constipation demands immediate, highly spec...
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Huntington Disease Genetic
1 testA family history of progressive movement, cognitive, and psychiatric decline is understandably daunting, but securing precise...
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Hyperoxaluria
2 testsExperiencing recurrent, severe kidney stones or unexplained kidney failure at a young age requires incredibly precise diagnos...
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Hypertension Genetics
2 testsStruggling with dangerously high blood pressure that strikes at a young age or completely resists standard medications is oft...
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Hypochondroplasia Genetic
1 testNavigating concerns about a child's disproportionate short stature or subtle skeletal differences requires compassionate, hig...
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Hypogonadotropic Hypogonadism
2 testsFacing delayed puberty, an absent sense of smell, or unexplained fertility challenges demands a deep look into the fundamenta...
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Ichthyosis Genetic
3 testsDealing with severe, chronic scaling, thickening, and extreme dryness of the skin from birth requires specialized diagnostic...
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Immunodeficiency
6 testsEnduring unusually severe, recurrent, or hard-to-treat infections demands a deep dive into the foundational defense mechanism...
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Immunodeficiency Disorders
1 testA complex history of immune system failures, overlapping autoimmune symptoms, and chronic infections warrants an expansive, h...
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Immunodeficiency Genetic
7 testsWhen clinical symptoms strongly point to a primary immune defect, getting a highly targeted genetic confirmation is the key t...
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Immunodeficiency Genetics
4 testsUnderstanding the broader hereditary factors affecting your immune resilience empowers you to make fully informed, proactive...
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Immunodeficiency Panel
2 testsConfronting overlapping infectious, autoinflammatory, and autoimmune symptoms demands a targeted, high-throughput diagnostic...
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Inherited Disorders
10 testsA family history of chronic illness, undiagnosed multi-system issues, or overlapping generational symptoms warrants proactive...
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Inherited Disorders Panel
1 testWhen clinical symptoms are ambiguous and point to multiple potential conditions across different organ systems, having access...
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Inherited Eye Disease Genetics
1 testUnderstanding the broader hereditary factors affecting your visual health empowers you to make proactive, highly informed dec...
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Inherited Eye Disorders
2 testsExperiencing early-onset vision changes, extreme light sensitivity, or navigating a family history of childhood blindness can...
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Inherited Genetic Disorders
2 testsEmpowering yourself with a deep understanding of your family’s hereditary history is the most effective way to protect your l...
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Inherited Immunodeficiency Disorders
1 testAddressing a family history of severe, life-threatening infections or unexplained autoimmune reactions demands highly specifi...
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Inherited Metabolic Diseases
1 testNavigating the complexities of inherited enzyme deficiencies requires rapid, high-resolution diagnostic insights to prevent t...
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Inherited Metabolic Disorders
23 testsDealing with sudden energy crises, severe muscle weakness, or unexplained organ dysfunction from childhood demands incredibly...
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Inherited Neurological Disorders
1 testCoping with the gradual onset of cognitive decline, severe neuropathies, or early-onset movement disorders is deeply unsettli...
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Inherited Neuromuscular Disorders
1 testExperiencing progressive muscle weakness, severe cramping, or delayed motor milestones in a child requires highly specific di...
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Inherited Skin Disorders
5 testsEnduring severe blistering, extreme scaling, or dangerous pigmentation issues from birth requires specialized diagnostic insi...
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Inherited Syndromes
1 testNavigating complex, overlapping physical, developmental, and intellectual symptoms in a child demands highly precise diagnost...
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Joubert Syndrome
2 testsConfronting low muscle tone, abnormal breathing patterns, or the distinct "molar tooth sign" on a brain MRI requires speciali...
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Leukemia Genetics
13 testsUncovering the exact molecular drivers of a blood cancer is essential for unlocking the most effective, targeted oncology tre...
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Leukodystrophy
1 testDealing with a child's progressive loss of motor skills, vision, or muscle control requires urgent, highly specific diagnosti...
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Leukodystrophy Gene
1 testWhen clinical imaging strongly suggests white matter deterioration, pinpointing the exact genetic mutation is crucial for unl...
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Leukodystrophy Genetic
1 testUnderstanding the broader hereditary factors behind myelin disorders empowers families to access proactive, specialized care...
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Lipid Disorders
1 testStruggling with dangerously high cholesterol or triglycerides that completely resist diet and exercise often signals a hidden...
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Lipid Metabolism Genetics
1 testA family history of early heart disease, severe metabolic imbalances, or sudden pancreatitis warrants a deep molecular look i...
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Lipodystrophy Genetic
1 testExperiencing an abnormal loss or accumulation of fat tissue, especially when paired with severe, early-onset insulin resistan...
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Long QT Syndrome
2 testsUnexplained fainting, severe palpitations, or a family history of sudden cardiac arrest requires immediate, life-saving diagn...
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Lymphoproliferative Disorders
1 testConfronting chronic swollen lymph nodes, an enlarged spleen, or an unexplained overproduction of immune cells demands rigorou...
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Lysosomal Storage Disorders Panel
1 testAddressing severe developmental regression, unexplained organ enlargement, or progressive skeletal changes in a child require...
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Mental Retardation Genetics
1 testSeeking answers for a child's unexplained intellectual disability or global developmental delays can be an emotional journey,...
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Metabolic Genetic
6 testsPinpointing the exact hereditary enzyme deficiency driving a metabolic crisis is the key to preventing irreversible damage an...
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Metabolic Genetic Disorders
11 testsUnderstanding the broader hereditary landscape of your body's energy production empowers you to manage chronic multi-system s...
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Metabolic Genetic Panel
1 testWhen complex symptoms point to a systemic energy failure, a high-throughput, targeted diagnostic approach is essential to bri...
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Metabolic Genetics
5 testsSecuring a deep, fundamental understanding of your family's metabolic blueprint allows for proactive, highly informed health...
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Microcephaly
1 testNavigating an abnormally small head circumference or restricted skull growth in an infant demands deeply compassionate, highl...
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Microcephaly Genetic
2 testsIdentifying the exact molecular mutation behind restricted brain development unlocks the most effective, specialized pediatri...
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Mitochondrial Disease
2 testsDealing with profound, unexplained muscle weakness, severe neurological decline, or multi-organ failure requires a deep look...
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Mitochondrial Disorders
62 testsComplex, overlapping symptoms that dramatically worsen with illness or metabolic stress often trace back to hidden hereditary...
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Mitochondrial DNA Depletion Syndromes
1 testDealing with profound muscle weakness, severe developmental regression, or early-onset liver failure in an infant requires ra...
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Mitochondrial Genetic
2 testsWhen overlapping, multi-system symptoms point to a fundamental cellular energy deficit, pinpointing the exact genetic mutatio...
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Mitochondrial Genetics
4 testsUnderstanding the broader hereditary factors affecting your cellular energy production empowers your family to make proactive...
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Molecular Genetics
18 testsAchieving a definitive diagnosis for complex, inherited conditions requires looking at the very foundation of your biological...
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Monogenic Diabetes
2 testsWhen diabetes strikes unusually early in life or doesn't fit the typical Type 1 or Type 2 profiles, uncovering a single-gene...
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Monogenic Disorders
4 testsA family history of a specific, inherited trait or chronic illness warrants proactive molecular insights to protect your futu...
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Mucolipidosis
1 testAddressing severe skeletal abnormalities, developmental delays, or progressive corneal clouding in a child demands highly spe...
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Mucopolysaccharidosis
3 testsDealing with progressive joint stiffness, enlarged organs, or distinctive skeletal changes in a child requires rapid, highly...
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Multiple Endocrine Neoplasia
1 testA family history of complex tumors in the thyroid, parathyroid, or adrenal glands warrants urgent, proactive molecular insigh...
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Muscular Dystrophy
14 testsCoping with progressive muscle weakness, frequent falls, or delayed motor milestones in a child requires highly specific diag...
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Muscular Dystrophy Genetic
7 testsWhen clinical signs strongly point to a specific neuromuscular breakdown, getting a targeted genetic confirmation is the key...
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Muscular Dystrophy Genetics
5 testsUnderstanding the broader hereditary factors affecting muscle integrity empowers families to access proactive, specialized ca...
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Myotonic Dystrophy
3 testsDealing with the inability to relax muscles after contraction (myotonia), alongside progressive weakness, cataracts, or cardi...
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Nephrolithiasis Genetic
1 testEnduring severe, recurrent kidney stones from a young age or a family history of progressive kidney damage warrants a deep mo...
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Nephrology Genetic
1 testA family history of chronic kidney disease, unexplained cysts, or progressive renal failure requires an expansive, high-resol...
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Nephronophthisis
3 testsAddressing unexplained excessive urination, extreme thirst, and progressive kidney failure in a child or young adult demands...
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Nephronophthisis Genetic
3 testsWhen clinical signs strongly point to a specific cystic kidney disease, getting a targeted genetic confirmation is the key to...
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Nephrotic Syndrome Genetic
1 testCoping with severe, persistent swelling, massive protein loss in the urine, and resistance to standard steroid treatments req...
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Neurodevelopmental Disorders
4 testsSeeking answers for a child's autism spectrum behaviors, intellectual disability, or global developmental delays can be an em...
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Neurogenetic
33 testsPinpointing the exact hereditary cause of a progressive movement disorder, severe neuropathy, or early-onset cognitive declin...
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Neurogenetic Disorders
25 testsUnderstanding the broader hereditary factors affecting your central and peripheral nervous systems empowers you to manage chr...
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Neurogenetics
68 testsSecuring a deep, fundamental understanding of your family's neurological blueprint allows for proactive, highly informed medi...
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Neurological Disorders
14 testsNavigating a family history of progressive, debilitating brain or nerve conditions warrants proactive, empowering insights to...
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Neurological Genetic
49 testsPinpointing the exact hereditary cause of a progressive movement disorder, severe neuropathy, or early-onset cognitive declin...
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Neurological Genetic Disorders
21 testsUnderstanding the broader hereditary factors affecting your central and peripheral nervous systems empowers you to manage chr...
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Neurological Genetics
71 testsSecuring a deep, fundamental understanding of your family's neurological blueprint allows for proactive, highly informed medi...
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Neuromuscular Disorders
14 testsCoping with progressive muscle weakness, frequent falls, or delayed motor milestones in a child requires highly specific diag...
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Neuromuscular Genetic
11 testsWhen clinical signs strongly point to a specific neuromuscular breakdown, getting a targeted genetic confirmation is the key...
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Neuromuscular Genetics
15 testsUnderstanding the broader hereditary factors affecting muscle and nerve integrity empowers families to access proactive, spec...
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The process
How Genetics testing works
A clear, four-step pathway from booking to a laboratory report you can share with your treating clinician.
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Step 1
Book your test
Reserve online or by phone. Our team confirms the investigation, the listed price and the right collection option for you.
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Step 2
Sample collection
Visit a collection centre or request home collection across Dubai and the UAE. Preparation instructions are shared in advance.
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Step 3
Laboratory analysis
Your sample is processed under documented quality controls, with chain-of-custody tracking from receipt to result.
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Step 4
Report & follow-up
Receive a secure digital report. Share it with your clinician, and contact our team if you need help understanding the next step.
Before your appointment
Preparation & sample collection
Follow the instructions you are given
Some investigations require fasting, a specific collection time, or avoiding certain medicines, supplements or strenuous activity. Instructions are confirmed when you book.
Bring your identification
A valid photo ID is required at collection so that your sample is matched correctly to your record.
Tell us about medicines
Let the team know about prescription medicines, supplements or recent procedures — these can affect how an investigation is scheduled or interpreted.
Ask if you are unsure
If anything about the preparation is unclear, contact us before your appointment rather than after collection — preparation errors can affect reporting times.
Patient information
Frequently asked questions
Practical answers about Genetics testing at DNA Labs UAE. This information is general and does not replace advice from your treating clinician.
What kinds of investigations are included in Genetics?
Genetics covers a group of laboratory investigations used to support assessment, diagnosis and monitoring. The right investigation depends on your symptoms, history and what your clinician is trying to establish, so selection should always be made with your treating doctor.
How do I book a Genetics test at DNA Labs UAE?
You can request a booking online or by phone. Our team confirms the investigation, the listed price, any preparation required and the collection option that suits you before anything is scheduled.
Do you offer home sample collection in Dubai and the UAE?
Yes. Home collection can be arranged across Dubai and the wider UAE. Appointment windows and coverage vary by location, so please confirm availability when you book.
How should I prepare for sample collection?
Preparation depends on the investigation. Some require fasting, a specific time of day, or avoiding certain medicines or activities beforehand. Please follow the instructions given at the time of booking and confirm anything unclear with your clinician or our laboratory team.
How long do results take?
Turnaround varies by investigation and method. The expected reporting time for your specific request is confirmed when you book.
How will I receive my report?
Reports are issued as secure digital documents. A copy can also be shared with your referring clinician on request. Please discuss the results with a qualified clinician, who can interpret them alongside your history and other findings.
Do I need a doctor's prescription?
Some investigations can be requested directly, while others require a referral from a licensed clinician. Our team will let you know what applies to your request before collection.
About this clinical information
The information on this Genetics page describes laboratory investigations in general terms. It is written to help you understand what an investigation involves — it is not a diagnosis and it is not a substitute for advice from your treating clinician.
- Investigation names, specimen types and listed prices are reviewed against laboratory records.
- Preparation guidance is indicative — confirm test-specific instructions before collection.
- Content is updated when investigations, methods or reporting formats change.
- Results are released to the patient and, on request, shared with the referring clinician.
Medical disclaimer: This page is for general information and education only. It is not medical advice, diagnosis or treatment, and it does not replace a consultation with a qualified healthcare professional. Always seek the advice of your doctor or another qualified provider with any questions about a medical condition or before ordering a test.
We're here to help
Speak to us about Genetics testing
Tell us what your clinician has requested and we'll confirm availability, price, preparation and the most convenient collection option — including home collection in Dubai and across the UAE.
- Home collection available across the UAE
- Digital reports delivered securely
- Confidential handling of every request