Karyotyping For Detection of Fragile X Syndrome
Introduction
Karyotyping for Detection of Fragile X Syndrome is a specialized genetic test that analyzes chromosomes to identify abnormalities that may lead to Fragile X Syndrome, a common inherited cause of intellectual disability. This test is particularly important for individuals with a family history of genetic disorders, as it helps in understanding genetic risks and planning for future health.
What the Test Measures
This test measures the number and structure of chromosomes in an individual’s cells, specifically looking for the fragile site on the X chromosome that is associated with Fragile X Syndrome. It helps to detect any chromosomal abnormalities that may affect mental and physical development.
Who Should Consider This Test?
Individuals who should consider the Karyotyping for Detection of Fragile X Syndrome include:
- Those with a family history of Fragile X Syndrome or other genetic disorders.
- Individuals displaying symptoms of intellectual disabilities or developmental delays.
- Parents who are carriers of the Fragile X mutation.
- Couples planning to conceive who want to assess genetic risks.
Benefits of Taking the Test
Taking the Karyotyping for Detection of Fragile X Syndrome test offers several benefits:
- Early identification of genetic disorders that can inform medical management.
- Guidance for family planning and genetic counseling.
- Peace of mind for individuals concerned about their genetic health.
- Access to tailored interventions and support for affected individuals.
Understanding Your Results
Results from the Karyotyping for Detection of Fragile X Syndrome will indicate whether any chromosomal abnormalities are present. A genetic counselor or healthcare provider will help interpret the results and discuss potential implications for health and family planning.
Test Information and Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| Karyotyping For Detection of Fragile X Syndrome | 150,000 NGN | 200,000 NGN |
Book Your Test Today!
Don’t wait to understand your genetic health. Book your Karyotyping for Detection of Fragile X Syndrome test today! For appointments, please call or WhatsApp us at +2348077798758.
Additional Information
Turnaround Time: 7-10 days
Sample Type: Peripheral blood
Test Components: Sodium Heparin Vacutainer (2ml)
Pre-Test Instructions: A Doctor’s prescription is required for this test. Please note that a prescription is not applicable for surgery and pregnancy cases or for individuals planning to travel abroad.
Specialty
This test is typically conducted by a Gynecologist specializing in genetics.
