NGS Single Gene tests in Dubai & UAE

Compare available NGS Single Gene 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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NGS Single Gene test prices

Showing 1–2 of 2 matching tests.

NGS Single Gene diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-2919 ANKH Gene Craniometaphyseal Dysplasia Genetic Test This test identifies pathogenic variants in the ANKH gene associated with Craniometaphyseal Dysplasia (CMD).	Whole Blood (EDTA), 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 ["Pathogenic variants in the ANKH gene"] Parameters [] Preparation ["Provide comprehensive clinical history", "Genetic counselling session required for pedigree chart"] Indications ["Suspected Craniometaphyseal Dysplasia (CMD)", "Family history of CMD", "Genetic counselling for at-risk individuals"] Measurement technique Confirm with laboratory Codes LOINC: 82810-7 ICD-10: Q78.8, Q75.8, Z13.79 Clinical summary This test identifies pathogenic variants in the ANKH gene associated with Craniometaphyseal Dysplasia (CMD).
TEST-4503 Loricrin (LOR) Gene Vohwinkel Syndrome with Ichthyosis Genetic Test This test identifies pathogenic variants in the LOR gene associated with Vohwinkel syndrome with ichthyosis.	Whole blood, extracted DNA, 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 LOR gene", "Copy number variations (CNV) in the LOR gene"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication without consulting your doctor"] Indications ["Clinical suspicion of Vohwinkel syndrome with ichthyosis", "Familial risk assessment for Vohwinkel syndrome"] Measurement technique Confirm with laboratory Codes Confirm with laboratory Clinical summary This test identifies pathogenic variants in the LOR gene associated with Vohwinkel syndrome with ichthyosis.

Category overview

NGS Single Gene: overview

When clinical symptoms strongly point toward a specific inherited condition, highly focused genetic testing provides the exact, rapid insights necessary for peace of mind. Integrated into our advanced Molecular Genetics services, NGS Single Gene testing meticulously analyzes one specific gene for known disease-causing mutations. Utilizing cutting-edge diagnostic technology, this highly focused molecular screening helps confirm or rule out precise genetic disorders, safely guiding targeted medical interventions and family planning strategies. Recognized for specialized diagnostic excellence among diagnostic labs in the UAE, DNA Labs ensures absolute patient confidentiality, exceptional analytical precision, and incredibly efficient turnaround times. Take an informed step forward in your health journey—schedule your NGS single gene testing in UAE, book a secure home sample collection, or reach out to our expert medical professionals.

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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.