Diagnostic options · UAE

Genetics tests in Dubai & UAE

Compare available Genetics tests, their listed prices and the information provided for each option. Test selection and preparation should be discussed with your clinician.

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2,789

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-1.00–50,000.00 AED

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Genetics test prices

Showing 2641–2655 of 2,789 matching tests.

Genetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-4102 TUBB2A Gene Cortical Dysplasia, Complex with Other Brain Malformations Type 5 Genetic Test This test identifies pathogenic variants in the TUBB2A gene associated with cortical dysplasia, complex with other brain malformations type 5.	Peripheral Whole Blood (2 EDTA tubes), FTA Card, or Extracted DNA	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["TUBB2A gene sequence", "Pathogenic variants in coding exons and splice sites"] Parameters [] Preparation ["No fasting required"] Indications ["Suspected cortical dysplasia, complex with other brain malformations type 5", "Drug-resistant epilepsy", "Family history of related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 21665-7 ICD-10: Q04.5 Clinical summary This test identifies pathogenic variants in the TUBB2A gene associated with cortical dysplasia, complex with other brain malformations type 5.
TEST-2541 TUBB2B Gene Microcephaly Genetic Test This test evaluates the TUBB2B gene for pathogenic variants associated with primary microcephaly.	Whole blood, extracted DNA, or FTA card (1 drop)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["TUBB2B gene sequence variants (SNVs, indels)", "TUBB2B gene copy number variations (CNVs)"] Parameters [] Preparation ["No fasting required", "Mandatory genetic counselling session prior to sample collection", "Provide complete clinical history of the proband", "Inform genetic counsellor of all current treatments"] Indications ["Suspected TUBB2B-related primary microcephaly", "Family history of TUBB2B-related microcephaly", "Need for genetic counselling regarding recurrence risk"] Measurement technique Confirm with laboratory Codes LOINC: 91868-9 ICD-10: Q02 Clinical summary This test evaluates the TUBB2B gene for pathogenic variants associated with primary microcephaly.
TEST-2437 TUBB2B Gene Polymicrogyria Asymmetric Genetic Test This test detects pathogenic variants in the TUBB2B gene associated with asymmetric polymicrogyria.	Whole blood, extracted DNA, or dried blood spot (FTA card)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the TUBB2B gene", "Single nucleotide variants", "Indels", "Copy number changes"] Parameters [] Preparation [] Indications ["Suspected diagnosis of asymmetric polymicrogyria", "Family history of TUBB2B-related disorders", "Genetic counseling for recurrence risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q04.3 Clinical summary This test detects pathogenic variants in the TUBB2B gene associated with asymmetric polymicrogyria.
TEST-4147 TUBB3 Gene Cortical Dysplasia, Complex, With Other Brain Malformations Type 1 Genetic Test This test identifies pathogenic variants in the TUBB3 gene associated with complex cortical dysplasia with other brain malformations type 1 (CDCBM1).	Peripheral Whole Blood	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in TUBB3 gene exons", "Pathogenic variants in TUBB3 gene splice junctions"] Parameters [] Preparation ["No specific fasting required", "Avoid allogeneic blood transfusion within the past 2 weeks"] Indications ["Suspected complex cortical dysplasia with other brain malformations type 1 (CDCBM1)", "Diagnostic odyssey in families with complex developmental brain malformations"] Measurement technique Confirm with laboratory Codes LOINC: 81313-5 ICD-10: Q04.8 Clinical summary This test identifies pathogenic variants in the TUBB3 gene associated with complex cortical dysplasia with other brain malformations type 1 (CDCBM1).
TEST-3626 TUBB3 Gene Sequencing for CFEOM3A Test This test detects pathogenic variants in the TUBB3 gene, which are associated with congenital fibrosis of extraocular muscles type 3A (CFEOM3A).	Whole Blood (Peripheral)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the TUBB3 gene"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medications"] Indications ["Suspected diagnosis of CFEOM3A", "Family history of CFEOM3A", "Genetic counselling for families with CFEOM3A"] Measurement technique Confirm with laboratory Codes LOINC: 59110-7 ICD-10: H49.81 Clinical summary This test detects pathogenic variants in the TUBB3 gene, which are associated with congenital fibrosis of extraocular muscles type 3A (CFEOM3A).
TEST-4682 TUBB4A Gene Leukodystrophy Hypomyelinating Type 6 Genetic Test This test identifies disease-causing mutations in the TUBB4A gene to confirm a molecular diagnosis of hypomyelinating leukodystrophy type 6.	Peripheral Whole Blood (3–5 mL in EDTA) or Buccal Swab	3–4 Weeks (expedited 10-day option available)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the TUBB4A gene"] Parameters [] Preparation ["Ensure child is well hydrated", "Topical anaesthetic cream may be applied if prescribed"] Indications ["Suspected hypomyelinating leukodystrophy type 6", "Family history of TUBB4A-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 21665-1 ICD-10: E75.23 Clinical summary This test identifies disease-causing mutations in the TUBB4A gene to confirm a molecular diagnosis of hypomyelinating leukodystrophy type 6.
TEST-5342 TUBG1 Gene Neurodevelopmental Malformation and Microcephaly Genetic Test This test identifies pathogenic variants in the TUBG1 gene, which are associated with autosomal dominant microcephaly and cortical brain malformations.	Peripheral Whole Blood (Venipuncture) or Dried Blood Spot (FTA Card)	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the TUBG1 gene", "Point mutations", "Small insertions and deletions", "Copy number variations"] Parameters [] Preparation [] Indications ["Infants and children with congenital microcephaly", "Individuals with cortical brain malformations", "Patients with global developmental delay", "Adults seeking molecular diagnosis for family planning"] Measurement technique Confirm with laboratory Codes LOINC: 101389-3 ICD-10: Q02, F79, Z13.79 Clinical summary This test identifies pathogenic variants in the TUBG1 gene, which are associated with autosomal dominant microcephaly and cortical brain malformations.
TEST-4493 TUFT1 Gene Tuftelin Deficiency Genetic Test This test evaluates the TUFT1 gene for mutations associated with tuftelin deficiency, which can cause enamel defects and immune system issues.	Peripheral whole blood (3–5 mL in EDTA tube) or saliva (Oragene kit)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["TUFT1 gene sequence", "Pathogenic variants in TUFT1"] Parameters [] Preparation [] Indications ["Amelogenesis imperfecta", "Enamel hypoplasia", "Immune-mediated syndromes", "Dermatological fragility"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: K00.5 Clinical summary This test evaluates the TUFT1 gene for mutations associated with tuftelin deficiency, which can cause enamel defects and immune system issues.
TEST-2915 TWIST1 Gene Craniosynostosis Type 1 Genetic Test This test evaluates the TWIST1 gene for pathogenic variants associated with craniosynostosis syndromes like Saethre-Chotzen syndrome.	Whole blood (EDTA), FTA card, or extracted DNA	3–4 weeks (expedited available)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the TWIST1 gene"] Parameters [] Preparation [] Indications ["Suspected Saethre-Chotzen syndrome", "Isolated craniosynostosis", "Paediatric differential diagnosis", "Surgical planning", "Family genetic counselling"] Measurement technique Confirm with laboratory Codes LOINC: 101261-4 ICD-10: Q75.0, Q87.0 Clinical summary This test evaluates the TWIST1 gene for pathogenic variants associated with craniosynostosis syndromes like Saethre-Chotzen syndrome.
TEST-2364 TWIST1 Gene Saethre-Chotzen Syndrome Genetic Test This test evaluates the TWIST1 gene for pathogenic variants associated with Saethre-Chotzen syndrome.	Peripheral Whole Blood (EDTA)	21–28 Business Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["TWIST1 gene sequence", "TWIST1 gene copy number variations (deletions/duplications)"] Parameters [{"name": "Diagnostic Sensitivity", "reference_range": "99.9%"}] Preparation ["No specific fasting required", "No medication or diet changes needed"] Indications ["Diagnosis of Saethre-Chotzen syndrome", "Prenatal diagnosis (if parental mutation identified)", "Family screening for at-risk members"] Measurement technique Confirm with laboratory Codes LOINC: 81264-7 ICD-10: Q87.0, Q75.0 Clinical summary This test evaluates the TWIST1 gene for pathogenic variants associated with Saethre-Chotzen syndrome.
TEST-2370 TWIST1 Gene Sequencing for Robinow‑Sorauf Syndrome (NGS) Test This test analyzes the TWIST1 gene to detect mutations associated with Robinow‑Sorauf syndrome, a rare autosomal dominant disorder.	Whole blood (3–5 mL in EDTA tube), or extracted DNA (5 µg minimum)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["TWIST1 gene sequence", "Single nucleotide variants", "Small insertions/deletions", "Copy number alterations"] Parameters [] Preparation ["Mandatory pre-test genetic counselling session"] Indications ["Suspected Robinow‑Sorauf syndrome", "Confirmation of diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 81307-2 ICD-10: Q87.0 Clinical summary This test analyzes the TWIST1 gene to detect mutations associated with Robinow‑Sorauf syndrome, a rare autosomal dominant disorder.
TEST-5537 TWNK (C10orf2) Gene Progressive External Ophthalmoplegia with Mitochondrial Deletions Type 3 Autosomal Dominant Genetic Test This genetic test analyzes the TWNK gene to detect mutations associated with Progressive External Ophthalmoplegia with Mitochondrial Deletions Type 3 (PEOA3).	Whole blood (EDTA), extracted DNA, or FTA card	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["TWNK gene sequence", "Copy number variants (CNVs) in TWNK gene"] Parameters [] Preparation [] Indications ["Clinical features of progressive external ophthalmoplegia", "Ptosis", "Mitochondrial myopathy", "Family history suggesting autosomal dominant inheritance"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: H49.81 Clinical summary This genetic test analyzes the TWNK gene to detect mutations associated with Progressive External Ophthalmoplegia with Mitochondrial Deletions Type 3 (PEOA3).
TEST-5815 TWNK Gene Infantile-Onset Spinocerebellar Ataxia (SCA) Genetic Test This genetic test identifies pathogenic variants within the TWNK gene associated with infantile-onset spinocerebellar ataxia.	Peripheral Whole Blood (1-2 mL) or FTA Card	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the TWNK gene", "Mitochondrial DNA replication defects"] Parameters [] Preparation ["Informed consent and a three-generation pedigree are mandatory prior to sample collection.", "Do not discontinue or alter prescribed medications without consulting the treating physician."] Indications ["Infants presenting with symptoms suggestive of infantile-onset spinocerebellar ataxia", "Family history of mitochondrial disorders", "Need for definitive molecular diagnosis for clinical management and genetic counseling"] Measurement technique Confirm with laboratory Codes LOINC: 94217-3 ICD-10: G11.0 Clinical summary This genetic test identifies pathogenic variants within the TWNK gene associated with infantile-onset spinocerebellar ataxia.
TEST-5206 TWNK Gene MTDPS7 Genetic Test This test identifies pathogenic variants in the TWNK gene associated with mitochondrial DNA depletion syndrome type 7 (MTDPS7).	Whole Blood (EDTA), FTA Card, or Extracted Genomic DNA	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the TWNK gene", "SNVs (Single Nucleotide Variants)", "Indels (Insertions/Deletions)", "CNVs (Copy Number Variants)"] Parameters [] Preparation ["No special preparation required", "Ensure patient is haemodynamically stable and afebrile before sample collection"] Indications ["Suspected mitochondrial DNA depletion syndrome type 7 (MTDPS7)", "Early clinical intervention", "Family planning", "Tailored neurological management"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: E88.49 Clinical summary This test identifies pathogenic variants in the TWNK gene associated with mitochondrial DNA depletion syndrome type 7 (MTDPS7).
TEST-5479 TWNK Gene Perrault Syndrome Type 5 Next-Generation Sequencing (NGS) Genetic Test This test identifies pathogenic variants in the TWNK gene, confirming a diagnosis of Perrault syndrome type 5.	Whole Blood (3–5 mL), Buccal Swab, or FTA Card	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the TWNK gene", "Single nucleotide variants", "Small insertions/deletions", "Copy number variations"] Parameters [] Preparation ["Pre-test genetic counseling is mandatory"] Indications ["Individuals with clinical features suggestive of Perrault syndrome", "Family history of Perrault syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q87.8 Clinical summary This test identifies pathogenic variants in the TWNK gene, confirming a diagnosis of Perrault syndrome type 5.

Category overview

Genetics: overview

Understanding your unique biological blueprint offers a profound sense of clarity and empowers proactive health planning for you and your family. At DNA Labs UAE, our specialized Genetics division employs state-of-the-art molecular technologies to provide deep insights into hereditary markers and cellular mutations. This comprehensive genetics testing in the UAE equips your healthcare provider with the precise data needed to tailor your medical guidance effectively. Recognized among top diagnostic labs in Dubai and the UAE, we prioritize your peace of mind through strict confidentiality protocols and exceptionally fast, accurate reporting. Take the next step in your health journey. View our genetics diagnostic services, book a private home collection, or consult our specialized team today.

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Genetics tests in Dubai & UAE

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