Biochemistry tests in Dubai & UAE

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

Tests in this category

1,113

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450.00–30,000.00 AED

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Biochemistry test prices

Showing 796–810 of 1,113 matching tests.

Biochemistry diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-5466 PMP22 Gene (HNPP) Next‑Generation Sequencing (NGS) Genetic Test This test identifies pathogenic variants within the PMP22 gene associated with Hereditary Neuropathy with Liability to Pressure Palsies (HNPP). It analyzes the full coding region,...	Whole Blood (2–3 mL in DNA preservation tube)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PMP22 gene sequence", "Copy Number Variations (CNVs) in PMP22", "Single Nucleotide Variants (SNVs)", "Small Insertions/Deletions (Indels)"] Parameters [] Preparation ["Completion of clinical history intake", "Mandatory pre-test genetic counseling session"] Indications ["Diagnosis confirmation of HNPP", "Identification of specific PMP22 variants", "Genetic counselling for affected families", "Risk assessment for family members"] Measurement technique Confirm with laboratory Codes LOINC: 81329-1 ICD-10: G60.8 Clinical summary This test identifies pathogenic variants within the PMP22 gene associated with Hereditary Neuropathy with Liability to Pressure Palsies (HNPP). It analyzes the full coding region, exon-intron boundaries, and copy number variations.
TEST-5448 PNKD Gene (Paroxysmal Nonkinesigenic Dyskinesia) Genetic Test This genetic test identifies pathogenic variants within the PNKD gene associated with paroxysmal nonkinesigenic dyskinesia.	Peripheral Whole Blood (3–5 mL in EDTA tube) 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 PNKD gene", "Copy number variants within the PNKD gene"] Parameters [] Preparation ["Genetic counseling session required before testing", "Full pedigree chart required"] Indications ["Suspected diagnosis of Paroxysmal Nonkinesigenic Dyskinesia", "Family history of PNKD"] Measurement technique Confirm with laboratory Codes LOINC: 94222-8 ICD-10: G24.8 Clinical summary This genetic test identifies pathogenic variants within the PNKD gene associated with paroxysmal nonkinesigenic dyskinesia.
TEST-4970 PNPLA1 Gene Sequencing for Autosomal Recessive Congenital Ichthyosis (ARCI) Test This test evaluates the PNPLA1 gene for variants associated with Autosomal Recessive Congenital Ichthyosis (ARCI). It identifies mutations within the gene's coding region.	Peripheral 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 ["PNPLA1 gene coding region variants", "Pathogenic mutations"] Parameters [] Preparation ["Mandatory pre-test genetic counselling session", "Provide family medical history and pedigree chart"] Indications ["Suspected diagnosis of Autosomal Recessive Congenital Ichthyosis (ARCI)", "Family history of ARCI", "Need for genetic counselling regarding ARCI risk"] Measurement technique Confirm with laboratory Codes LOINC: 81263-5 ICD-10: Q80.8, Q80.9 Clinical summary This test evaluates the PNPLA1 gene for variants associated with Autosomal Recessive Congenital Ichthyosis (ARCI). It identifies mutations within the gene's coding region.
TEST-2628 POLD1 Gene Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy (MDPL) Syndrome Genetic Test This test analyzes the POLD1 gene to identify pathogenic variants associated with Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy (MDPL) syndrome.	Whole Blood (EDTA), Extracted DNA, or Buccal Swab	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["POLD1 gene sequence variants", "Pathogenic mutations"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Suspected MDPL syndrome", "Family history of MDPL syndrome", "Guidance for clinical management", "Family planning"] Measurement technique Confirm with laboratory Codes LOINC: 82307-3 ICD-10: E88.1, Q75.8, H90.3 Clinical summary This test analyzes the POLD1 gene to identify pathogenic variants associated with Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy (MDPL) syndrome.
TEST-5615 POLG Gene Progressive External Ophthalmoplegia with Mitochondrial Deletions Type 1, Autosomal Dominant (Genetic Test) This genetic test detects pathogenic variants in the POLG gene associated with autosomal dominant progressive external ophthalmoplegia with mitochondrial deletions type 1 (PEOA1).	Peripheral Whole Blood, DNA FTA Card, or Extracted DNA	21 – 28 Business Days (3 – 4 Weeks)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["POLG gene variants (SNVs, indels, CNVs)", "Mitochondrial DNA deletion hotspots"] Parameters [] Preparation ["No specific fasting required", "Continue all prescribed medications"] Indications ["Suspected PEOA1 based on clinical presentation", "Family history of mitochondrial disorders", "Need for definitive molecular diagnosis", "Cascade screening of at-risk relatives"] Measurement technique Confirm with laboratory Codes LOINC: 82989-5 ICD-10: H49.4 Clinical summary This genetic test detects pathogenic variants in the POLG gene associated with autosomal dominant progressive external ophthalmoplegia with mitochondrial deletions type 1 (PEOA1).
TEST-4685 POLR3B Gene Leukodystrophy Hypomyelinating Type 8 Genetic Test This genetic test identifies pathogenic variants in the POLR3B gene associated with hypomyelinating leukodystrophy type 8.	Whole Blood (EDTA), Extracted DNA (≥1 µg), or FTA Card Dried Blood Spot	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["POLR3B gene variants", "Single-nucleotide variants", "Small insertions/deletions", "Splice-site alterations"] Parameters [] Preparation ["Pre-test genetic counselling is mandatory", "Obtain informed consent"] Indications ["Diagnosis of hypomyelinating leukodystrophy type 8", "Confirmation of clinical suspicion"] Measurement technique Confirm with laboratory Codes LOINC: 21643-2 ICD-10: E75.2 Clinical summary This genetic test identifies pathogenic variants in the POLR3B gene associated with hypomyelinating leukodystrophy type 8.
TEST-2927 Pompe Disease Quantitative Blood Test This diagnostic test evaluates the activity level of the acid α-glucosidase (GAA) enzyme in whole blood.	Whole blood (EDTA or lithium heparin)	4 working days	700.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Acid α-glucosidase (GAA) enzyme activity"] Parameters [{"name": "Acid α-glucosidase (GAA) Enzyme Activity", "reference_range": null}] Preparation ["No specific fasting required", "Continue all prescribed medications"] Indications ["Suspicion of Pompe disease (Glycogen Storage Disease Type II)", "Evaluation of muscle weakness", "Assessment of cardiomyopathy", "Investigation of respiratory insufficiency"] Measurement technique Confirm with laboratory Codes LOINC: 24617-9 ICD-10: E74.02 Clinical summary This diagnostic test evaluates the activity level of the acid α-glucosidase (GAA) enzyme in whole blood.
TEST-5267 POMT2 Gene Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies), Type A2, Genetic Test This genetic test identifies mutations in the POMT2 gene associated with congenital muscular dystrophy-dystroglycanopathy type A2 (MDDGA2).	Whole Blood 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 ["Mutations in the POMT2 gene", "Single nucleotide variants", "Indels", "Copy number variations"] Parameters [] Preparation ["No specific fasting required", "No medication or diet restrictions"] Indications ["Individuals with clinical symptoms of MDDGA2", "Family members of affected individuals for carrier status determination"] Measurement technique Confirm with laboratory Codes LOINC: 83580-5 ICD-10: G71.2 Clinical summary This genetic test identifies mutations in the POMT2 gene associated with congenital muscular dystrophy-dystroglycanopathy type A2 (MDDGA2).
TEST-5970 POR Gene (Cytochrome P450 Oxidoreductase Deficiency) Adrenal Hyperplasia Genetic Test This genetic test evaluates the POR gene for pathogenic variants associated with cytochrome P450 oxidoreductase deficiency, a form of congenital adrenal hyperplasia.	Whole Blood, Extracted DNA, or 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 POR gene", "Presence of mutations causing cytochrome P450 oxidoreductase deficiency"] Parameters [] Preparation ["Prior genetic counselling session required", "Fasting is not required", "A simple blood or DNA sample collection is needed"] Indications ["Diagnosis of congenital adrenal hyperplasia (CAH)", "Evaluation of ambiguous genitalia", "Investigation of cortisol deficiency", "Assessment of skeletal malformations"] Measurement technique Confirm with laboratory Codes LOINC: 101404-8 ICD-10: E25.0, E25.8, Z13.228 Clinical summary This genetic test evaluates the POR gene for pathogenic variants associated with cytochrome P450 oxidoreductase deficiency, a form of congenital adrenal hyperplasia.
TEST-5097 PORCN Gene Focal Dermal Hypoplasia Genetic Test This test evaluates the PORCN gene for mutations associated with Focal Dermal Hypoplasia (Goltz syndrome).	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 mutations in the PORCN gene", "Single nucleotide variants", "Small insertions/deletions", "Copy number changes"] Parameters [{"name": "Gene Coverage", "reference_range": "Full coding region + splice sites ±10 bp"}, {"name": "Sensitivity", "reference_range": ">99.9% for point mutations & small indels"}] Preparation ["No fasting required", "Pre-test genetic counseling recommended"] Indications ["Documented clinical suspicion of Goltz syndrome", "Family history of Goltz syndrome", "Genetic counseling for affected families"] Measurement technique Confirm with laboratory Codes LOINC: 96507-0 ICD-10: Q87.2 Clinical summary This test evaluates the PORCN gene for mutations associated with Focal Dermal Hypoplasia (Goltz syndrome).
TEST-2931 Porphobilinogen (PBG) Quantitative 24-Hour Urine Test This test measures the quantitative level of porphobilinogen in a 24-hour urine collection to diagnose acute hepatic porphyrias.	24-Hour Urine (Light-Protected Collection)	Same Day (if sample received by 9 AM)	850.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Porphobilinogen (PBG) levels", "Heme biosynthesis pathway intermediates"] Parameters [{"name": "Porphobilinogen (PBG)", "reference_range": null}] Preparation ["Collect all urine for 24 hours in a dark container", "Avoid light exposure at all times", "Discard first morning urine", "Refrigerate sample during collection", "Do not discontinue prescribed medications without consulting physician"] Indications ["Suspected acute hepatic porphyria (AIP, VP, HCP)", "Monitoring therapy effectiveness", "Differentiating acute attacks from secondary causes"] Measurement technique Confirm with laboratory Codes LOINC: 14842-9 ICD-10: E80.21, E80.2 Clinical summary This test measures the quantitative level of porphobilinogen in a 24-hour urine collection to diagnose acute hepatic porphyrias.
TEST-2929 Porphobilinogen (PBG), Qualitative, Urine Test This test detects pathologically elevated Porphobilinogen (PBG) in urine, a key indicator of acute intermittent porphyria (AIP), variegate porphyria, and hereditary coproporphyria.	Random Urine	Same Day (Sample by 9 AM Tue/Fri)	850.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Porphobilinogen (PBG) levels", "Presence of porphyrin precursor"] Parameters [{"name": "Porphobilinogen (PBG)", "reference_range": "Qualitative: Positive/Negative"}] Preparation ["Avoid alcohol for at least 48 hours prior", "Inform physician about all current medications"] Indications ["Suspected acute intermittent porphyria (AIP)", "Suspected variegate porphyria", "Suspected hereditary coproporphyria", "Evaluation of acute neurovisceral symptoms"] Measurement technique Confirm with laboratory Codes LOINC: 2811-5 ICD-10: E80.2, E80.1, E80.0, Z15.89 Clinical summary This test detects pathologically elevated Porphobilinogen (PBG) in urine, a key indicator of acute intermittent porphyria (AIP), variegate porphyria, and hereditary coproporphyria.
TEST-2934 Porphyrins Total Qualitative Random Urine Test This test qualitatively assesses the presence of elevated total porphyrins in a random urine sample.	Random Urine	Same Day (within hours)	900.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Total Porphyrins in Urine"] Parameters [{"name": "Total Porphyrins", "reference_range": "Qualitative (Positive/Negative)"}] Preparation ["Collect a random urine sample during acute symptoms into a light-protected container provided by the laboratory.", "No preservatives or special dietary preparations are required."] Indications ["Suspected acute porphyria during symptomatic episodes"] Measurement technique Confirm with laboratory Codes LOINC: 2072-3 ICD-10: E80.2 Clinical summary This test qualitatively assesses the presence of elevated total porphyrins in a random urine sample.
TEST-2936 Porphyrins Total Quantitative 24‑Hour Urine Test This diagnostic test evaluates the total concentration of porphyrins excreted in the urine over a 24-hour period.	24-Hour Urine	Same day (sample received by 1 pm)	900.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Total Porphyrins", "Metabolite levels in urine"] Parameters [{"name": "Total Porphyrins", "reference_range": null}] Preparation ["Collect all urine voided over a full 24-hour period.", "Keep the container refrigerated at all times.", "Record the total urine volume accurately.", "Provide a full medication list to the laboratory."] Indications ["Screening for porphyria disorders", "Monitoring porphyria disorders", "Investigating unexplained neurological symptoms", "Evaluating patients with suspected metabolic abnormalities"] Measurement technique Confirm with laboratory Codes LOINC: 20276-6 ICD-10: E80.20, R82.99 Clinical summary This diagnostic test evaluates the total concentration of porphyrins excreted in the urine over a 24-hour period.
TEST-6113 PPARG Gene Lipodystrophy, Familial Partial, Type 3 Genetic Test This test identifies pathogenic variants in the PPARG gene associated with Familial Partial Lipodystrophy Type 3 (FPLD3).	Whole Blood (EDTA) or DNA 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 PPARG gene"] Parameters [] Preparation [] Indications ["Diagnosis of Familial Partial Lipodystrophy Type 3 (FPLD3)", "Assessment of eligibility for metreleptin therapy", "Familial cascade screening for FPLD3"] Measurement technique Confirm with laboratory Codes LOINC: 81315-3 ICD-10: E88.1 Clinical summary This test identifies pathogenic variants in the PPARG gene associated with Familial Partial Lipodystrophy Type 3 (FPLD3).

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Biochemistry: overview

Seeking clarity about your body's essential functions is vital for long-term well-being. At DNA Labs UAE, our Biochemistry services utilize advanced automated analyzers to evaluate enzymes, proteins, and metabolites in your blood. Whether you need routine metabolic panels or specialized biochemical testing in the UAE, these tests provide critical data to guide your physician's medical plan. As a leading diagnostic lab in Dubai and the UAE, we guarantee strict confidentiality and rapid, accurate turnaround times. Take charge of your health today. Explore our biochemistry diagnostics below, schedule a convenient home sample collection, or contact our specialists to book your test.

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Biochemistry tests in Dubai & UAE

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