Genetics tests in Dubai & UAE

This test detects pathogenic variants in the CATSPER1 gene associated with spermatogenic failure type 7 and male infertility.

This test evaluates the CATSPER2 gene for pathogenic variants associated with autosomal recessive syndromic hearing loss and male sterility.

This diagnostic test evaluates the entire coding region and splice sites of the CATSPER2 gene for pathogenic variants linked to deafness and male infertility.

This genetic test evaluates the CAV3 gene for pathogenic variants linked to familial hypertrophic cardiomyopathy.

This test identifies pathogenic variants in the CAV3 gene associated with Long QT Syndrome Type 9.

This test identifies mutations in the CAV3 gene associated with elevated serum creatine kinase levels and related neuromuscular disorders.

This test identifies pathogenic variants in the CAV3 gene, confirming a diagnosis of Limb-Girdle Muscular Dystrophy Type 1C (LGMD1C).

This genetic test identifies mutations in the CAVIN1 gene associated with Congenital Generalized Lipodystrophy Type 4 (CGL4).

This test evaluates the CBFB gene for pathogenic variants associated with skeletal dysplasias and dysmorphology.

This test detects the presence or absence of the CBFB-MYH11 fusion transcript, a specific genetic abnormality associated with a favorable prognosis in acute myeloid leukemia.

This test identifies germline mutations in the CBL gene associated with an increased risk of developing Juvenile Myelomonocytic Leukemia (JMML).

This test identifies pathogenic variants in the CC2D1A gene associated with Autosomal Recessive Intellectual Disability Type 3 (MRT3).

This test analyzes the CC2D2A gene for variants associated with COACH syndrome.

This diagnostic test evaluates the CC2D2A gene for pathogenic variants associated with Joubert syndrome type 9.

This genetic test detects pathogenic DNA variants in the entire coding region of the CCBE1 gene, confirming the molecular cause of Hennekam syndrome type 1.