FISH Microdeletion Detection for Williams Syndrome Test
Introduction
The FISH Microdeletion Detection for Williams Syndrome Test is a specialized genetic test that uses Fluorescence In Situ Hybridization (FISH) technology to identify microdeletions on chromosome 7, which are associated with Williams Syndrome. This condition is characterized by developmental delays, cardiovascular problems, and distinct facial features. Early detection is crucial for effective management and intervention.
What the Test Measures
This test specifically detects microdeletions in the 7q11.23 region of chromosome 7, which are indicative of Williams Syndrome. By analyzing the genetic material, healthcare providers can confirm or rule out the presence of this genetic disorder.
Who Should Consider This Test?
Individuals who may benefit from this test include:
- Children and adults displaying developmental delays or learning difficulties.
- Individuals with a family history of genetic disorders.
- Patients with cardiovascular issues without a clear cause.
- Parents expecting a child with potential genetic risks.
Benefits of Taking the Test
Taking the FISH Microdeletion Detection for Williams Syndrome Test offers several benefits:
- Early diagnosis can lead to timely interventions and support.
- Helps families understand the genetic basis of conditions affecting their loved ones.
- Provides clarity for medical management and care strategies.
- Offers peace of mind for individuals and families concerned about genetic disorders.
Understanding Your Results
Results from the FISH Microdeletion Detection for Williams Syndrome Test are typically available within 4 working days. A positive result indicates the presence of the genetic deletion associated with Williams Syndrome, while a negative result suggests that the deletion is not present. It is essential to discuss results with a healthcare provider to understand the implications and next steps.
Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| FISH Microdeletion Detection for Williams Syndrome Test | 17,000 KSh | 24,000 KSh |
Sample Collection and Instructions
The test requires a sample of 5 mL (3 mL min.) of whole blood collected in a Green Top (Sodium Heparin) tube. It should be shipped at a temperature of 18-22°C and must not be frozen. Additionally, a duly filled Chromosome & FISH Analysis Requisition Form (Form 17) is mandatory for processing.
Branches Across Kenya
We have branches in all major cities in Kenya, including Nairobi, Mombasa, and Kisumu, and we offer home sample collection services for your convenience.
Book Your Test Today!
Don’t wait! Ensure peace of mind for you and your family. Call or WhatsApp us at +254711564616 to book the FISH Microdeletion Detection for Williams Syndrome Test today!
