Fragile X (FMR1) Mutation Screen (L)
AED3,400.00
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.
Description
Fragile X (FMR1) Mutation Screen (L)
Unlock critical genetic insights with the Fragile X (FMR1) Mutation Screen (L)—a cutting-edge diagnostic test designed to detect mutations in the FMR1 gene, the primary cause of Fragile X syndrome (FXS). This highly accurate screening tool identifies CGG repeat expansions within the FMR1 gene, providing essential information for individuals and families concerned about intellectual disabilities, developmental delays, and associated conditions.
### Key Features:
✔ Comprehensive Genetic Analysis – Detects normal, premutation, and full mutation expansions in the FMR1 gene, offering a complete risk assessment.
✔ Advanced Molecular Technology – Utilizes state-of-the-art PCR and Southern blot techniques for precise and reliable results.
✔ Early Detection & Risk Assessment – Ideal for individuals with a family history of Fragile X syndrome, unexplained developmental delays, or autism spectrum disorders.
✔ Carrier Screening for Women – Essential for women considering pregnancy, as Fragile X is an X-linked disorder that can be passed to offspring.
✔ Fast & Confidential Results – Ensures timely reporting to support informed medical decisions and genetic counseling.
### Why Choose This Test?
The Fragile X (FMR1) Mutation Screen (L) empowers individuals, families, and healthcare providers with critical genetic knowledge. Early detection allows for proactive intervention, personalized treatment planning, and informed reproductive choices. Whether you are seeking answers for developmental concerns or planning for the future, this test delivers clarity and confidence.
Take control of your genetic health today with the Fragile X (FMR1) Mutation Screen (L)—because knowledge is the first step toward better outcomes.
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