WDPCP Gene Bardet-Biedl Syndrome Type 15 NGS Genetic DNA Test
Introduction
The WDPCP Gene Bardet-Biedl Syndrome Type 15 NGS Genetic DNA Test is a specialized diagnostic tool designed to identify mutations in the WDPCP gene, which are associated with Bardet-Biedl syndrome. This syndrome is a rare genetic disorder that can lead to a variety of health issues, including obesity, kidney problems, and vision loss. Early detection through genetic testing can significantly improve patient outcomes.
What the Test Measures
This genetic test utilizes Next Generation Sequencing (NGS) technology to analyze the WDPCP gene. It detects specific mutations that may predispose individuals to Bardet-Biedl syndrome type 15, allowing for a comprehensive understanding of genetic risks.
Who Should Consider This Test
Individuals with:
- A family history of Bardet-Biedl syndrome
- Symptoms such as obesity, retinal dystrophy, polydactyly, and renal abnormalities
- Known genetic predispositions to related conditions
Benefits of Taking the Test
- Provides clarity on genetic risks and predispositions
- Enables early intervention and management of potential health issues
- Informs family planning decisions
- Facilitates personalized treatment options based on genetic insights
Understanding Your Results
Results from the WDPCP Gene Bardet-Biedl Syndrome Type 15 NGS Genetic DNA Test will indicate whether mutations are present in the WDPCP gene. A genetic counseling session is recommended to help interpret the results and discuss potential implications for health and family.
Test Pricing
Test Name | Discount Price (NGN) | Regular Price (NGN) |
---|---|---|
WDPCP Gene Bardet-Biedl Syndrome Type 15 NGS Genetic DNA Test | 400000 | 560000 |
Book Your Test Today!
Don’t wait to gain valuable insights into your genetic health. Contact us today to book the WDPCP Gene Bardet-Biedl Syndrome Type 15 NGS Genetic DNA Test. Call or WhatsApp us at +2348077798758.
Additional Information
- Turnaround Time: 3 to 4 Weeks
- Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
- Pre-Test Instructions: Clinical History of Patient who is going for the test and a Genetic Counselling session to draw a pedigree chart of family members affected with the syndrome.
- Specialty: General Physician
- Department: Genetics
- Method: NGS Technology
- Disease Type: Hepatology Nephrology Endocrinology Disorders