Fragile X Syndrome FMR1 Detection by PCR
Introduction
The Fragile X Syndrome FMR1 Detection by PCR is a specialized genetic test that identifies mutations in the FMR1 gene, which is responsible for Fragile X Syndrome. This condition is the most common inherited cause of intellectual disability and is associated with various developmental and behavioral issues. Understanding the genetic basis of Fragile X Syndrome is crucial for early diagnosis, management, and counseling.
What the Test Measures
This test specifically detects the number of CGG repeats in the FMR1 gene. A normal gene has up to 44 repeats, while individuals with Fragile X Syndrome typically have more than 200 repeats, leading to the silencing of the gene.
Who Should Consider This Test
Individuals who may consider this test include:
- Those with a family history of Fragile X Syndrome or related disorders.
- Individuals showing symptoms such as developmental delays, learning disabilities, or behavioral issues.
- Women who are planning a pregnancy and wish to understand their genetic risks.
- Men and women with a known family history of FMR1 mutations.
Benefits of Taking the Test
The benefits of undergoing the Fragile X Syndrome FMR1 Detection by PCR include:
- Early identification of at-risk individuals and families.
- Informed reproductive choices based on genetic risks.
- Access to appropriate interventions and support services for affected individuals.
- Peace of mind for families concerning their genetic health.
Understanding Your Results
Results from the Fragile X Syndrome FMR1 Detection by PCR will indicate whether the FMR1 gene is normal, premutation, or fully mutated. It is essential to consult with a healthcare professional to interpret these results accurately and to understand the implications for health and family planning.
Test Information and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Fragile X Syndrome FMR1 Detection by PCR | 160,000 NGN | 200,000 NGN |
Booking the Test
To book the Fragile X Syndrome FMR1 Detection by PCR, please ensure you have a Doctor’s prescription. Note that this test is not applicable for individuals undergoing surgery or pregnancy, or those planning to travel abroad. For inquiries or to schedule your test, call or WhatsApp us at +2348077798758.
Take the first step towards understanding your genetic health today!
