FMR1 Gene Fragile X Syndrome NGS Genetic DNA Test
Introduction to the FMR1 Gene Fragile X Syndrome NGS Genetic DNA Test
The FMR1 Gene Fragile X Syndrome NGS Genetic DNA Test is an essential diagnostic tool used to identify mutations in the FMR1 gene, which are responsible for Fragile X syndrome—a leading cause of inherited intellectual disability. This test employs Next-Generation Sequencing (NGS) technology, providing accurate and comprehensive genetic analysis.
What the Test Measures
This test specifically measures the number of CGG repeats in the FMR1 gene. A normal gene has 5 to 44 repeats, while 55 to 200 repeats indicate a premutation, and over 200 repeats signify a full mutation, leading to Fragile X syndrome.
Who Should Consider This Test
Individuals who should consider the FMR1 Gene Fragile X Syndrome NGS Genetic DNA Test include:
- Those with a family history of Fragile X syndrome or intellectual disabilities.
- Individuals displaying symptoms of developmental delays, learning disabilities, or behavioral issues.
- Expectant parents who wish to understand their genetic risk for passing on Fragile X syndrome.
Benefits of Taking the Test
Taking the FMR1 Gene Fragile X Syndrome NGS Genetic DNA Test offers several benefits:
- Early identification of at-risk individuals, allowing for timely intervention and support.
- Informed family planning decisions for prospective parents.
- Access to tailored therapeutic strategies and educational resources for affected individuals.
Understanding Your Results
Results from the FMR1 Gene Fragile X Syndrome NGS Genetic DNA Test will indicate whether the FMR1 gene is normal, a premutation, or a full mutation. It is crucial to consult with a qualified healthcare professional to interpret the results accurately and discuss potential next steps.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| FMR1 Gene Fragile X Syndrome NGS Genetic DNA Test | 400000 NGN | 560000 NGN |
Book Your Test Today!
To book the FMR1 Gene Fragile X Syndrome NGS Genetic DNA Test, please contact us at +2348077798758 or visit our website for more information. Don’t wait—take the first step towards understanding your genetic health today!
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: Clinical History of Patient who is going for FMR1 Gene Fragile X Syndrome NGS Genetic DNA Test; A Genetic Counselling session to draw a pedigree chart of family members affected with FMR1 Gene Fragile X syndrome.
Specialty and Department
This test is conducted by specialists in the fields of Neurology and Genetics, employing advanced NGS Technology to ensure the highest standards of accuracy and reliability in diagnosing Neurological Disorders.
