FISH Prader Willi Syndrome SNRPN Test
Introduction to the FISH Prader Willi Syndrome SNRPN Test
The FISH (Fluorescence In Situ Hybridization) Prader Willi Syndrome SNRPN Test is a specialized genetic test designed to detect chromosomal abnormalities associated with Prader-Willi syndrome (PWS). This condition is characterized by a range of symptoms including hypotonia, obesity, intellectual disability, and behavioral problems. Early diagnosis through this test is crucial for effective management and intervention.
What the Test Measures
This test specifically measures the presence or absence of genetic material from the SNRPN gene located on chromosome 15, which is critical in the diagnosis of Prader-Willi syndrome. By identifying deletions or alterations in this gene, healthcare providers can confirm a diagnosis and guide treatment options.
Who Should Consider This Test?
Individuals who may benefit from the FISH Prader Willi Syndrome SNRPN Test include:
- Infants or children showing symptoms of PWS such as poor muscle tone, feeding difficulties, and developmental delays.
- Individuals with a family history of genetic disorders.
- Patients with unexplained obesity or behavioral issues.
Benefits of Taking the Test
Taking the FISH Prader Willi Syndrome SNRPN Test offers several advantages:
- Early diagnosis and management of Prader-Willi syndrome.
- Informed decision-making regarding treatment options.
- Access to support and resources for families affected by PWS.
Understanding Your Results
Results from the FISH Prader Willi Syndrome SNRPN Test will typically be available within four working days. A positive result may indicate the presence of Prader-Willi syndrome, while a negative result suggests that the genetic abnormality is not present. It is essential to consult with a healthcare provider to interpret the results accurately and discuss further steps.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| FISH Prader Willi Syndrome SNRPN Test | 18,000 KSh | 30,000 KSh |
Sample Collection and Instructions
The sample required for this test is 5 mL (3 mL minimum) of whole blood collected in a Green Top (Sodium Heparin) tube. It is essential to ship the sample at 18-22°C and to complete the Chromosome & FISH analysis Requisition Form (Form 17) before submission. Please do not freeze the sample.
Branches and Home Sample Collection
DNA Labs Kenya has branches across all major cities in Kenya, making it convenient for you to access our services. We also offer home sample collection services for your convenience.
Book Your Test Today!
Don’t wait to get the answers you need. Book the FISH Prader Willi Syndrome SNRPN Test today by calling or WhatsApping us at +254711564616. Your health is our priority!
