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Diagnostic options · UAE

Inherited Genetic Disorders tests in Dubai & UAE

Compare available Inherited Genetic Disorders 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

2

Listed price range

2,800.00 AED

Clinical preparation

Confirm test-specific instructions with your clinician or laboratory.

Compare available tests

Inherited Genetic Disorders test prices

Showing 1–2 of 2 matching tests.

Inherited Genetic Disorders diagnostic tests, details, and listed prices
Test and description Specimen Typical duration Price Options
TEST-5402
ITGB6 Gene Amelogenesis Imperfecta Type 1H Genetic Test

This test analyzes the ITGB6 gene for mutations associated with Amelogenesis Imperfecta Type 1H, a condition affecting tooth enamel and potentially skin and immune function.

Peripheral whole blood (3–5 mL in EDTA tube) 3–4 weeks from sample receipt 2,800.00 AED
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View test specifications and preparation
What it measures
["Pathogenic variants in the ITGB6 gene", "Exonic regions and splice-site boundaries of ITGB6"]
Parameters
[]
Preparation
["No fasting required", "Pre-test genetic counselling session mandatory"]
Indications
["Suspected Amelogenesis Imperfecta Type 1H", "Family history of Amelogenesis Imperfecta Type 1H", "Need for definitive molecular diagnosis"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 94808-8 ICD-10: K00.4
Clinical summary
This test analyzes the ITGB6 gene for mutations associated with Amelogenesis Imperfecta Type 1H, a condition affecting tooth enamel and potentially skin and immune function.
TEST-5975
PEX14 Gene Zellweger Syndrome Genetic Test

This test analyzes the PEX14 gene for mutations associated with Zellweger syndrome spectrum disorders.

Whole Blood (EDTA), Extracted DNA, or Dried Blood Spot (FTA card) 3–4 Weeks 2,800.00 AED
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View test specifications and preparation
What it measures
["Single-nucleotide variants in PEX14 gene", "Small insertions/deletions in PEX14 gene", "Copy-number alterations in PEX14 gene"]
Parameters
[]
Preparation
["No specific fasting required", "No medication or diet changes needed"]
Indications
["Suspected Zellweger syndrome spectrum disorder", "Need for definitive molecular diagnosis", "Reproductive risk assessment", "Guiding clinical management"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 21636-6 ICD-10: E71.510
Clinical summary
This test analyzes the PEX14 gene for mutations associated with Zellweger syndrome spectrum disorders.

Category overview

Inherited Genetic Disorders: overview

Empowering yourself with a deep understanding of your family’s hereditary history is the most effective way to protect your long-term systemic wellness and secure absolute reproductive confidence. As a core pillar of our advanced Molecular Genetics department, testing for Inherited Genetic Disorders evaluates your DNA for a curated selection of mutations known to cause distinct, multi-system congenital conditions. By leveraging cutting-edge sequencing technology, this empowering molecular screening provides the critical clarity needed to assess personal risks and carrier status, safely guiding informed family planning, proactive medical interventions, and specialized reproductive counseling. Widely respected for compassionate diagnostic excellence among premier diagnostic labs in Dubai and the UAE, DNA Labs ensures strict patient confidentiality, uncompromising diagnostic precision, and highly efficient reporting. Take control of your personalized healthcare journey—book your inherited genetic disorders testing in UAE, arrange a seamless clinic or home sample collection, or consult our dedicated medical genetics professionals.

Before booking

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.