Metabolic Genetics tests in Dubai & UAE

Compare available Metabolic 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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Listed price range

2,800.00 AED

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Metabolic Genetics test prices

Showing 1–5 of 5 matching tests.

Metabolic Genetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-6045 ACACA Gene Acetyl-CoA Carboxylase Deficiency Genetic Test This genetic test analyzes the ACACA gene for variants associated with Acetyl-CoA Carboxylase Deficiency.	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 the ACACA gene", "Fatty acid biosynthesis pathway"] Parameters [] Preparation ["No fasting required", "Pre-test genetic counseling session provided"] Indications ["Suspected Acetyl-CoA Carboxylase Deficiency", "Family history of metabolic disorders"] Measurement technique Confirm with laboratory Codes LOINC: 102361-9 ICD-10: E88.8 Clinical summary This genetic test analyzes the ACACA gene for variants associated with Acetyl-CoA Carboxylase Deficiency.
TEST-6059 HADHA Gene Sequencing Test (LCHAD Deficiency) This test evaluates the HADHA gene for pathogenic variants associated with Long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency.	Peripheral Whole Blood (EDTA), Extracted DNA, or Dried Blood Spot (FTA Card)	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 HADHA gene", "Single nucleotide variants (SNVs)", "Insertions/deletions (indels)", "Copy number variations (CNVs)"] Parameters [] Preparation ["Provide a detailed clinical history of the patient.", "Mandatory pre-genetic counselling session (in-person or telehealth).", "No fasting required.", "Inform the laboratory if the patient has had a blood transfusion or bone marrow transplant in the preceding two weeks."] Indications ["Symptomatic infants suspected of LCHAD deficiency", "Confirmation of diagnosis in individuals with abnormal acylcarnitine profiles", "Carrier screening in families with a history of LCHAD deficiency", "Pre-implantation genetic diagnosis (PGD) or prenatal diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 81235-6 ICD-10: E71.310 Clinical summary This test evaluates the HADHA gene for pathogenic variants associated with Long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency.
TEST-5902 PDP1 Gene Pyruvate Dehydrogenase Phosphatase Deficiency Genetic Test This genetic test identifies pathogenic variants in the PDP1 gene, confirming pyruvate dehydrogenase phosphatase deficiency.	Peripheral whole blood, extracted DNA, 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 ["Pathogenic variants in the PDP1 gene"] Parameters [] Preparation [] Indications ["Clinical signs of lactic acidosis", "Neurological regression", "Family history suggesting PDP1 deficiency"] Measurement technique Confirm with laboratory Codes LOINC: 21620-7 ICD-10: E74.42 Clinical summary This genetic test identifies pathogenic variants in the PDP1 gene, confirming pyruvate dehydrogenase phosphatase deficiency.
TEST-5875 PSAT1 Gene NGS Test for Phosphoserine Aminotransferase Deficiency This test identifies pathogenic variants in the PSAT1 gene, confirming a diagnosis of phosphoserine aminotransferase deficiency.	Peripheral whole blood, extracted DNA, or FTA card specimen	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 PSAT1 gene", "Coding exons and splice junctions"] Parameters [] Preparation ["No specific patient preparation required"] Indications ["Unexplained developmental delay", "Microcephaly", "Seizures", "Biochemical evidence of serine deficiency", "Asymptomatic siblings of affected individuals"] Measurement technique Confirm with laboratory Codes LOINC: 94236-7 ICD-10: E72.8 Clinical summary This test identifies pathogenic variants in the PSAT1 gene, confirming a diagnosis of phosphoserine aminotransferase deficiency.
TEST-5894 SLC52A1 Gene Riboflavin Deficiency Genetic Test This test identifies pathogenic variants in the SLC52A1 gene, which cause riboflavin transporter deficiency type 1, a treatable neurometabolic disorder.	Peripheral Whole Blood (EDTA) or DNA 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 SLC52A1 gene", "Single-nucleotide variants", "Small insertions/deletions", "Copy-number changes"] Parameters [] Preparation ["Genetic counselling with a certified geneticist is mandatory before sample collection"] Indications ["Suspected riboflavin transporter deficiency type 1", "Infant-onset neurological decline", "Carrier screening"] Measurement technique Confirm with laboratory Codes LOINC: 94835-3 ICD-10: E53.0 Clinical summary This test identifies pathogenic variants in the SLC52A1 gene, which cause riboflavin transporter deficiency type 1, a treatable neurometabolic disorder.

Category overview

Metabolic Genetics: overview

Securing a deep, fundamental understanding of your family's metabolic blueprint allows for proactive, highly informed health decisions that protect your long-term vitality. As a core pillar of our advanced Molecular Genetics department, comprehensive Metabolic Genetics screening provides an in-depth evaluation of the complex hereditary pathways that govern cellular energy and waste management. Utilizing advanced genomic technology, this expansive profiling helps identify hidden molecular risks long before symptoms escalate, safely guiding your healthcare provider in tailoring highly personalized preventative care, customized biochemical therapies, and proactive family planning. Recognized for preventative diagnostic excellence among top diagnostic labs in Dubai and the UAE, DNA Labs ensures strict patient confidentiality, unparalleled diagnostic accuracy, and prompt, reliable reporting. Take an empowered step toward targeted wellness—book your metabolic genetics testing in UAE, arrange a secure clinic or home sample collection, or connect with our specialized medical team today.

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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.