Congenital Disorders of Glycosylation tests in Dubai & UAE

Compare available Congenital Disorders of Glycosylation 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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Congenital Disorders of Glycosylation test prices

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Congenital Disorders of Glycosylation diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-6363 ALG2 Gene Glycosylation Disorder Type 1I Genetic Test This genetic test identifies pathogenic variants in the ALG2 gene associated with congenital disorder of glycosylation type 1I (CDG‑1I). It confirms the molecular basis of this rar...	Whole Blood (EDTA tube 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 ALG2 gene", "Congenital disorder of glycosylation type 1I (CDG‑1I)"] Parameters [] Preparation ["No fasting required", "No specific medication or diet restrictions"] Indications ["Suspected congenital disorder of glycosylation type 1I (CDG‑1I)", "Family history of CDG‑1I", "Unexplained multi-systemic symptoms suggestive of a metabolic disorder"] Measurement technique Confirm with laboratory Codes LOINC: 94219-5 ICD-10: E77.8 Clinical summary This genetic test identifies pathogenic variants in the ALG2 gene associated with congenital disorder of glycosylation type 1I (CDG‑1I). It confirms the molecular basis of this rare metabolic disorder.
TEST-4470 B4GALT1 Gene Sequencing (CDG Type IId) Test This test identifies disease-causing mutations in the B4GALT1 gene, providing a definitive molecular diagnosis for Congenital Disorder of Glycosylation Type IId.	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 ["B4GALT1 gene sequence", "Copy Number Variations (CNVs) in B4GALT1"] Parameters [] Preparation ["No specific fasting required", "Ensure informed consent is obtained"] Indications ["Suspected Congenital Disorder of Glycosylation Type IId (CDG Type IId)", "Patients with unexplained neurological impairment, hypotonia, or developmental delay"] Measurement technique Confirm with laboratory Codes LOINC: 48000-4 ICD-10: E77.8 Clinical summary This test identifies disease-causing mutations in the B4GALT1 gene, providing a definitive molecular diagnosis for Congenital Disorder of Glycosylation Type IId.

Category overview

Congenital Disorders of Glycosylation: overview

Dealing with unexplained developmental delays or multi-organ metabolic symptoms in a child can be deeply concerning, but uncovering the precise genetic root provides profound reassurance. Under our Molecular Diagnostics umbrella, our testing for Congenital Disorders of Glycosylation employs state-of-the-art genomic sequencing to safely detect inherited mutations affecting cellular sugar attachment. Rather than delivering a final standalone diagnosis, this specialized genetic data equips your pediatric specialist with the crucial molecular insights needed for tailored, proactive medical guidance. As one of the most respected diagnostic labs in Dubai and the UAE, DNA Labs UAE guarantees strict patient confidentiality and incredibly fast, highly accurate turnaround times. Empower your family's metabolic health journey: explore our congenital disorders of glycosylation testing in the UAE below to book your appointment, schedule a gentle home collection, or consult 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.