Molecular Genetics tests in Dubai & UAE

Compare available Molecular Genetics 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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Molecular Genetics test prices

Showing 16–18 of 18 matching tests.

Molecular Genetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-3935 TBX19 Gene Adrenocorticotropic Hormone Deficiency Genetic Test This genetic test identifies pathogenic variants in the TBX19 gene associated with congenital isolated ACTH deficiency.	Whole Blood 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 TBX19 gene"] Parameters [] Preparation [] Indications ["Suspected congenital isolated ACTH deficiency", "Family history of ACTH deficiency"] Measurement technique Confirm with laboratory Codes LOINC: 94083-0 ICD-10: E23.0 Clinical summary This genetic test identifies pathogenic variants in the TBX19 gene associated with congenital isolated ACTH deficiency.
TEST-2883 WAC Gene Desanto-Shinawi Syndrome Genetic Test This genetic test analyzes the WAC gene for pathogenic variants associated with Desanto-Shinawi Syndrome.	Whole Blood (EDTA), Extracted DNA, or FTA Card	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 WAC gene", "Single nucleotide variants (SNVs)", "Insertions and deletions (indels)", "Copy number variations (CNVs)"] Parameters [] Preparation [] Indications ["Clinical suspicion of Desanto-Shinawi Syndrome", "Evaluation of developmental delay with dysmorphic features"] Measurement technique Confirm with laboratory Codes LOINC: 92822-6 ICD-10: Q87.8 Clinical summary This genetic test analyzes the WAC gene for pathogenic variants associated with Desanto-Shinawi Syndrome.
TEST-2841 WNT7A Gene Sequencing for Fibular Aplasia/Hypoplasia, Femoral Bowing & Polydactyly (NGS) Test This test identifies pathogenic variants in the WNT7A gene associated with fibular aplasia/hypoplasia, femoral bowing, and polydactyly.	Peripheral blood (or extracted DNA; FTA card accepted for infants)	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 WNT7A gene"] Parameters [] Preparation [] Indications ["Neonates or children presenting with fibular hypoplasia/aplasia", "Femoral bowing", "Extra digits", "Family history suggesting autosomal dominant or recessive pattern with limb anomalies"] Measurement technique Confirm with laboratory Codes LOINC: 21836-0 ICD-10: Q72.4 Clinical summary This test identifies pathogenic variants in the WNT7A gene associated with fibular aplasia/hypoplasia, femoral bowing, and polydactyly.

Category overview

Molecular Genetics: overview

Achieving a definitive diagnosis for complex, inherited conditions requires looking at the very foundation of your biological code. As the cornerstone of our advanced laboratory services, the Molecular Genetics department utilizes state-of-the-art sequencing and targeted DNA analysis to uncover the precise genetic mutations driving rare diseases, inherited cancers, and complex metabolic disorders. By leveraging cutting-edge molecular technology, this expansive profiling helps establish an absolute diagnosis, safely guiding your healthcare provider in tailoring highly personalized precision medicine, targeted therapies, and specialized reproductive counseling. Consistently ranked among the best diagnostic labs in the UAE, DNA Labs guarantees strict patient confidentiality, uncompromising diagnostic accuracy, and highly efficient turnaround times. Prioritize your personalized healthcare journey—schedule your molecular genetics testing in UAE, coordinate a seamless home sample collection, or consult our expert medical genetics team.

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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.