FISH Prader Willi Syndrome SNRPN Test
Introduction
The FISH Prader Willi Syndrome SNRPN Test is a specialized genetic test designed to detect abnormalities in the SNRPN gene associated with Prader-Willi Syndrome (PWS). This genetic disorder is characterized by a range of symptoms, including developmental delays, obesity, and behavioral issues. Early diagnosis through this test is crucial for effective management and intervention, allowing for better health outcomes and improved quality of life for affected individuals.
What the Test Measures
This test uses Fluorescence In Situ Hybridization (FISH) technology to analyze the SNRPN gene located on chromosome 15. It detects deletions or mutations that may be responsible for Prader-Willi Syndrome. By identifying these genetic changes, healthcare providers can confirm a diagnosis and tailor treatment plans accordingly.
Who Should Consider This Test
Parents or guardians should consider the FISH Prader Willi Syndrome SNRPN Test if their child exhibits symptoms such as:
- Developmental delays
- Feeding difficulties
- Excessive weight gain
- Behavioral problems
Additionally, individuals with a family history of genetic disorders may also benefit from this test.
Benefits of Taking the Test
- Early diagnosis of Prader-Willi Syndrome
- Informed decision-making regarding treatment options
- Access to specialized care and resources
- Improved management of symptoms and associated conditions
Understanding Your Results
Results from the FISH Prader Willi Syndrome SNRPN Test will typically be available within four working days after sample submission. A positive result indicates the presence of genetic abnormalities associated with Prader-Willi Syndrome, while a negative result suggests that no such abnormalities were detected. It is essential to discuss results with a healthcare professional to understand the implications fully.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 180,000 |
| Regular Price | 300,000 |
Book Your Test Today!
To schedule the FISH Prader Willi Syndrome SNRPN Test, please call or WhatsApp us at +2348077798758. Ensure your child receives the best care through early detection and management of genetic disorders.
Test Details
- Turnaround Time: Sample Daily by 4 pm; Report in 4 Working Days
- Sample Type: 5 mL (3 mL min.) whole blood from 1 Green Top (Sodium Heparin) tube. Ship at 18-22°C. DO NOT FREEZE. Duly filled Chromosome & FISH analysis Requisition Form (Form 17) is mandatory.
- Pre-Test Instructions: Duly filled Chromosome & FISH analysis Requisition Form (Form 17) is mandatory.
- Specialty: Pediatrician
- Department: Cytogenetics
- Method: FISH
- Disease Type: Genetic Disorders
