Fragile X FMR1 Carrier Test
Introduction
The Fragile X FMR1 Carrier Test is a genetic test that detects mutations in the FMR1 gene, which is responsible for Fragile X syndrome, a leading cause of inherited intellectual disability. This test is crucial for individuals who have a family history of Fragile X syndrome or related genetic disorders, as it can provide essential information for family planning and risk assessment.
What the Test Measures
This test measures the number of CGG repeats in the FMR1 gene. A normal gene has up to 44 repeats, while 55 to 200 repeats indicate a premutation, which can lead to Fragile X syndrome in offspring. Individuals with over 200 repeats are considered to have the full mutation.
Who Should Consider This Test?
Individuals who should consider the Fragile X FMR1 Carrier Test include:
- Those with a family history of Fragile X syndrome or intellectual disabilities.
- Parents or prospective parents concerned about passing on genetic disorders.
- Individuals with symptoms suggesting Fragile X syndrome.
Benefits of Taking the Test
Taking the Fragile X FMR1 Carrier Test offers several benefits:
- Provides clarity on genetic risks for future children.
- Enables informed family planning decisions.
- Helps in understanding the potential health implications for family members.
Understanding Your Results
Results will indicate whether you are a carrier of the FMR1 gene mutation. A positive result may warrant further genetic counseling to discuss implications and next steps. It’s essential to consult with a healthcare provider to interpret your results accurately.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Fragile X FMR1 Carrier Test | 240,000 NGN | 360,000 NGN |
Book Your Test Today!
To ensure your health and the health of your future family, book the Fragile X FMR1 Carrier Test today. For inquiries or to schedule your appointment, call or WhatsApp us at +2348110567037. Our team at DNA Labs Nigeria is here to assist you with your diagnostic needs.
