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Beta Thalassemia by PCR is a molecular diagnostic test designed to detect mutations in the HBB gene responsible for beta thalassemia.
Sample Type : EDTA Whole Blood
Methodology : PCR
TAT : 4 Weeks
The Fragile X (FMR1) Mutation Screen (L) is a genetic test designed to detect mutations in the FMR1 gene, which are associated with Fragile X syndrome, a leading cause of inherited intellectual disability and autism. This screening identifies CGG repeat expansions, distinguishing between normal, premutation, and full mutation alleles. Key benefits include early detection for informed reproductive decisions, risk assessment for carriers, and guidance for personalized medical management. Utilizing advanced molecular techniques, the test ensures high accuracy and reliability. Ideal for individuals with a family history of Fragile X or unexplained developmental delays, this screening provides critical genetic insights for proactive healthcare planning.
Detect Fragile-X Syndrome with a lab test that identifies FMR1 gene mutations linked to intellectual disability and developmental delays.
Sample Type : Whole Blood
Methodology : Direct Mutation Analysis by PCR and Southern Blot Analysis
TAT : 30 Days
Get the SMA Genetic Test in Dubai to detect SMN1 gene mutations. Early screening for newborns & couples. Accurate, fast results. Book your test today!
