Karyotyping For Detection of Fragile X Syndrome
Introduction to Karyotyping
Karyotyping for Detection of Fragile X Syndrome is a specialized genetic test that allows for the identification of chromosomal abnormalities associated with Fragile X Syndrome, a common inherited cause of intellectual disability. This test is vital for early diagnosis and management of individuals who may be affected by this condition.
What the Test Measures
This test measures the number and structure of chromosomes in a sample of peripheral blood. It specifically looks for the presence of the FMR1 gene mutation that causes Fragile X Syndrome. The analysis is performed using cell culture techniques to provide accurate results.
Who Should Consider This Test?
Individuals who should consider this test include:
- Those with a family history of Fragile X Syndrome or other genetic disorders.
- Individuals showing symptoms of intellectual disabilities.
- Parents with a child diagnosed with Fragile X Syndrome.
- Women planning pregnancy who are concerned about genetic risks.
Benefits of Taking the Test
Taking the Karyotyping test offers numerous benefits, including:
- Early detection of Fragile X Syndrome, allowing for timely interventions.
- Informed family planning decisions for those at risk.
- Access to support and resources for affected individuals and families.
- Peace of mind for individuals concerned about genetic conditions.
Understanding Your Results
Results from the Karyotyping test will be available within 7-10 days. A healthcare provider will interpret the results, explaining any chromosomal abnormalities detected and their implications. It is essential to discuss the findings with a gynecologist or a genetic counselor for comprehensive understanding and guidance.
Test Pricing
| Test Name | Discount Price (KSh) | Regular Price (KSh) |
|---|---|---|
| Karyotyping For Detection of Fragile X Syndrome | 15,000 | 20,000 |
Booking Your Test
We have branches across all major cities in Kenya, making it convenient for you to access our services. To book your Karyotyping for Detection of Fragile X Syndrome test, please call or WhatsApp us at +254711564616. Ensure you have a Doctor’s prescription before the test, as it is required for the procedure. Note that prescriptions are not applicable for those undergoing surgery, pregnancy, or planning to travel abroad.
Take the first step towards understanding your genetic health today!
