Peroxisomal Disorders tests in Dubai & UAE

Compare available Peroxisomal 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

Clinical preparation

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Peroxisomal Disorders test prices

Showing 1–2 of 2 matching tests.

Peroxisomal Disorders diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-5467 PEX1 Gene Peroxisome Biogenesis Disorder Type 1B Genetic Test This genetic test identifies pathogenic variants in the PEX1 gene associated with peroxisome biogenesis disorder type 1B.	Whole blood (Venous) or FTA card sample	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 PEX1 gene", "Single nucleotide variants (SNVs)", "Small insertions/deletions (indels)"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Suspected peroxisome biogenesis disorder type 1B", "Carrier testing", "Prenatal planning"] Measurement technique Confirm with laboratory Codes LOINC: 48006-3 ICD-10: E71.510 Clinical summary This genetic test identifies pathogenic variants in the PEX1 gene associated with peroxisome biogenesis disorder type 1B.
TEST-5979 PEX19 Gene Zellweger Syndrome Genetic Test This test identifies pathogenic variants in the PEX19 gene associated with Zellweger spectrum disorders.	Whole Blood (Peripheral) or Extracted DNA or Dried Blood Spot	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PEX19 gene variants", "Peroxisomal biogenesis disorder"] Parameters [] Preparation ["Genetic counseling is mandatory prior to sample collection."] Indications ["Diagnosis of Zellweger spectrum disorder", "Carrier screening", "Prenatal diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 62869-5 ICD-10: E71.510 Clinical summary This test identifies pathogenic variants in the PEX19 gene associated with Zellweger spectrum disorders.

Category overview

Peroxisomal Disorders: overview

Confronting complex neurological and metabolic symptoms in a newborn or young child demands urgent, precise clarity to ensure they receive the most effective specialized care. Within our elite Genetics department, testing for Peroxisomal Disorders maps specific genetic mutations that disrupt cellular metabolism and waste disposal, such as those seen in Zellweger syndrome. Utilizing advanced diagnostic technology, this crucial molecular screening helps identify these rare cellular dysfunctions, providing the definitive data necessary to safely guide targeted metabolic therapies and specialized pediatric oversight. Highly regarded for sensitive pediatric genetic care among diagnostic labs in Dubai and the UAE, DNA Labs guarantees strict patient confidentiality, unparalleled diagnostic accuracy, and highly efficient turnaround times. Secure the critical diagnostic insights your family deserves—book your peroxisomal disorders testing in UAE, coordinate a secure sample collection, or reach out to our dedicated 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.