Genetic for Metabolic Disorders tests in Dubai & UAE

Compare available Genetic for 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 for Metabolic Disorders test prices

Showing 1–4 of 4 matching tests.

Genetic for Metabolic Disorders diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-6382 ALDOB Gene Hereditary Fructose Intolerance (HFI) Genetic Test This genetic test identifies disease-causing variants in the ALDOB gene, confirming hereditary fructose intolerance (HFI). It assesses the entire coding region and splice sites for...	Whole Blood (3 mL) or FTA Micro-Collection Card	3 – 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ALDOB gene sequence", "Pathogenic variants in ALDOB gene"] Parameters [] Preparation ["Detailed clinical history recording required", "Mandatory genetic counselling session", "Three-generation pedigree documentation"] Indications ["Clinical suspicion of hereditary fructose intolerance", "Family history of HFI or unexplained liver disease", "Need for definitive molecular diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 94228-2 ICD-10: E74.12 Clinical summary This genetic test identifies disease-causing variants in the ALDOB gene, confirming hereditary fructose intolerance (HFI). It assesses the entire coding region and splice sites for mutations.
TEST-6032 CLPB Gene (3-Methylglutaconic Aciduria Type 7) with Cataracts, Neurologic Involvement and Neutropenia Test This genetic test identifies disease-causing variants in the CLPB gene associated with 3-methylglutaconic aciduria type 7 (MGCA7).	Whole Blood (EDTA), FTA Card, or Extracted DNA (Saliva acceptable)	21 – 28 Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the CLPB gene", "Deletion/Duplication analysis of the CLPB gene"] Parameters [] Preparation ["No specific fasting required", "Avoid recent blood transfusions if possible"] Indications ["Suspected 3-methylglutaconic aciduria type 7 (MGCA7)", "Family history of MGCA7"] Measurement technique Confirm with laboratory Codes LOINC: 94051-1 ICD-10: E71.19 Clinical summary This genetic test identifies disease-causing variants in the CLPB gene associated with 3-methylglutaconic aciduria type 7 (MGCA7).
TEST-6281 COG7 Gene Congenital Disorder of Glycosylation Type IIe (CDG‑IIe) Genetic Test This test evaluates the COG7 gene for mutations associated with Congenital Disorder of Glycosylation Type IIe (CDG-IIe). It identifies single nucleotide variants and exonic deletio...	Whole blood (EDTA), 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 ["COG7 gene sequence", "Copy Number Variations (CNV) in COG7"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication"] Indications ["Suspected Congenital Disorder of Glycosylation Type IIe (CDG-IIe)", "Family history of CDG-IIe"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: E77.8 Clinical summary This test evaluates the COG7 gene for mutations associated with Congenital Disorder of Glycosylation Type IIe (CDG-IIe). It identifies single nucleotide variants and exonic deletions.
TEST-5938 NAGLU Gene Sequencing for Mucopolysaccharidosis Type IIIB (Sanfilippo B) Test This test evaluates the NAGLU gene for pathogenic variants associated with Mucopolysaccharidosis Type IIIB (Sanfilippo B).	Peripheral Whole Blood (EDTA tube, 3-5 mL)	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 NAGLU gene", "Coding exons and flanking intronic regions"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Suspected diagnosis of Mucopolysaccharidosis Type IIIB (Sanfilippo B)", "Family history of MPS IIIB", "Carrier screening in families with a history of MPS IIIB"] Measurement technique Confirm with laboratory Codes LOINC: 94147-2 ICD-10: E76.22 Clinical summary This test evaluates the NAGLU gene for pathogenic variants associated with Mucopolysaccharidosis Type IIIB (Sanfilippo B).

Category overview

Genetic for Metabolic Disorders: overview

Addressing sudden metabolic crises, unexplained developmental delays, or severe lethargy in a newborn demands rapid, highly specific diagnostic intervention to prevent irreversible damage. Representing a critical component of our Genetics and Pediatrics departments, testing Genetic for Metabolic Disorders evaluates your child's DNA for inherited enzyme deficiencies that disrupt the body’s ability to process proteins, fats, or carbohydrates (Inborn Errors of Metabolism). By leveraging state-of-the-art diagnostic technology, this life-saving molecular screening provides the definitive clarity needed to safely guide immediate, highly customized dietary restrictions, medical formulas, and specialized metabolic management. Widely respected for sensitive pediatric diagnostics among top diagnostic labs in the UAE, DNA Labs guarantees absolute patient confidentiality, uncompromising diagnostic accuracy, and incredibly fast turnaround times. Safeguard your child's physiological health—schedule your genetic for metabolic disorders testing in UAE, coordinate a secure clinical sample collection, or reach out to our expert pediatric specialists.

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Use the test details as a conversation starter

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.