Genetic Metabolic Disorders tests in Dubai & UAE

Compare available Genetic Metabolic Disorders 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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Listed price range

2,800.00 AED

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Genetic Metabolic Disorders test prices

Showing 1–3 of 3 matching tests.

Genetic Metabolic Disorders diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-6235 ABCC8 Gene Transient Neonatal Diabetes Mellitus Type 2 Genetic Test This test identifies pathogenic variants in the ABCC8 gene associated with transient neonatal diabetes mellitus type 2.	Whole Blood (EDTA) or Dried Blood Spot	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 ABCC8 gene"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of any medications"] Indications ["Diagnosis of transient neonatal diabetes mellitus type 2", "Differentiation from permanent neonatal diabetes"] Measurement technique Confirm with laboratory Codes LOINC: 82237-3 ICD-10: P70.2 Clinical summary This test identifies pathogenic variants in the ABCC8 gene associated with transient neonatal diabetes mellitus type 2.
TEST-6086 AMPD3 Gene AMP Deaminase Deficiency (Erythrocytic) Genetic Test This genetic test identifies pathogenic variants in the AMPD3 gene associated with erythrocytic adenosine monophosphate deaminase deficiency.	Peripheral whole blood (EDTA)	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 AMPD3 gene", "SNVs, indels, CNVs"] Parameters [] Preparation ["Do not discontinue, modify, or skip any prescribed medication or supplement in preparation for this test.", "Consult your treating physician first."] Indications ["Symptomatic patients", "At-risk families", "Health-optimisation seekers", "Diagnosis of hereditary AMP deaminase deficiency"] Measurement technique Confirm with laboratory Codes LOINC: 96778-1 ICD-10: D55.2 Clinical summary This genetic test identifies pathogenic variants in the AMPD3 gene associated with erythrocytic adenosine monophosphate deaminase deficiency.
TEST-6060 CPT1B (Carnitine Palmitoyltransferase 1B) Deficiency Genetic Test via Next‑Generation Sequencing (NGS) This genetic test evaluates the CPT1B gene for pathogenic variants associated with Carnitine Palmitoyltransferase 1B deficiency.	Whole Blood (EDTA) or FTA Card Blood Spot	3–4 weeks including genetic counselling	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the CPT1B gene", "Variant allele frequency"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication"] Indications ["Suspected CPT1B deficiency", "Family screening for CPT1B deficiency", "Recurrent muscle symptoms"] Measurement technique Confirm with laboratory Codes LOINC: 81321-5 ICD-10: E71.314 Clinical summary This genetic test evaluates the CPT1B gene for pathogenic variants associated with Carnitine Palmitoyltransferase 1B deficiency.

Category overview

Genetic Metabolic Disorders: overview

Addressing unexplained fatigue, developmental delays, or complex metabolic symptoms can be highly stressful, but securing precise genetic answers empowers smarter health decisions. Situated within our Molecular Diagnostics division, our Genetic Metabolic Disorders testing leverages cutting-edge DNA sequencing to identify inherited variations affecting how your body processes energy. Rather than an absolute diagnosis, this detailed genetic metabolic disorders data acts as a powerful tool for your endocrinologist, offering the molecular clarity required for personalized medical guidance. As one of the leading diagnostic labs in the UAE, DNA Labs UAE guarantees uncompromising patient privacy and exceptionally swift, meticulous results. Take charge of your metabolic well-being: explore our genetic metabolic disorders testing in the UAE below to book an appointment, arrange a gentle home collection, or speak with our experts.

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The right diagnostic option depends on your reason for testing and individual circumstances. Check the listed specimen and timing, then confirm any preparation requirements with the ordering clinician or laboratory before collection.