Hyperoxaluria tests in Dubai & UAE

Compare available Hyperoxaluria 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

Listed price range

2,800.00 AED

Clinical preparation

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Hyperoxaluria test prices

Showing 1–2 of 2 matching tests.

Hyperoxaluria diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-6218 AGXT Gene (Hyperoxaluria Type 1) Next-Generation Sequencing (NGS) Genetic Test This test screens for pathogenic variants in the AGXT gene associated with primary hyperoxaluria type 1.	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 AGXT gene", "Single Nucleotide Variants (SNVs)", "Insertions/Deletions (indels)", "Copy Number Variants (CNVs)"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication without consulting your doctor"] Indications ["Confirmation of primary hyperoxaluria type 1 diagnosis", "Carrier screening in at-risk individuals"] Measurement technique Confirm with laboratory Codes LOINC: 82931-7 ICD-10: E74.8, Z15.02, Z14.8 Clinical summary This test screens for pathogenic variants in the AGXT gene associated with primary hyperoxaluria type 1.
TEST-6157 GRHPR Gene Hyperoxaluria Type 2 Genetic Test This genetic test analyzes the GRHPR gene for mutations associated with primary hyperoxaluria type 2.	Whole Blood or Buccal Swab	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 GRHPR gene", "Full gene coverage analysis"] Parameters [] Preparation ["Genetic counseling is mandatory before sample collection.", "Provide a three-generation family pedigree if possible."] Indications ["Suspected primary hyperoxaluria type 2", "Recurrent nephrolithiasis", "Family history of hyperoxaluria"] Measurement technique Confirm with laboratory Codes LOINC: 101616-2 ICD-10: E72.53 Clinical summary This genetic test analyzes the GRHPR gene for mutations associated with primary hyperoxaluria type 2.

Category overview

Hyperoxaluria: overview

Experiencing recurrent, severe kidney stones or unexplained kidney failure at a young age requires incredibly precise diagnostic clarity to halt irreversible renal damage. Representing an elite diagnostic tool in our Genetics and Nephrology services, Hyperoxaluria testing evaluates your DNA for inherited enzyme deficiencies (such as mutations in the AGXT or GRHPR genes) that cause the toxic overproduction of oxalate. By leveraging advanced sequencing technology, this life-saving molecular screening confirms Primary Hyperoxaluria, offering the definitive data necessary to safely guide aggressive hydration therapies, targeted vitamin B6 treatments, and critical organ transplant planning. Highly regarded for complex metabolic diagnostics among premier diagnostic labs in Dubai and the UAE, DNA Labs ensures strict patient confidentiality, unparalleled diagnostic accuracy, and prompt, reliable reporting. Protect your renal stability—book your hyperoxaluria testing in UAE, arrange a secure clinical sample transfer, or connect with our specialized medical genetics 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.