FLCN Gene BirtHoggDube Syndrome NGS Genetic DNA Test
Introduction to the Test
The FLCN Gene BirtHoggDube Syndrome NGS Genetic DNA Test is an advanced diagnostic tool designed to detect mutations in the FLCN gene, which are associated with Birt-Hogg-Dube syndrome. This genetic condition is characterized by skin tumors, lung cysts, and an increased risk of kidney cancer. Early detection through this test is crucial for effective management and prevention of serious health issues.
What the Test Measures
This test utilizes Next-Generation Sequencing (NGS) technology to analyze the FLCN gene. It identifies specific genetic mutations that could lead to the development of Birt-Hogg-Dube syndrome. Understanding these mutations helps in assessing the risk for patients and their families.
Who Should Consider This Test?
Individuals with a family history of Birt-Hogg-Dube syndrome or those exhibiting symptoms such as:
- Skin lesions or tumors
- Lung cysts
- Kidney tumors
are advised to consider this test. Additionally, patients with dysmorphology concerns may benefit from genetic counseling and testing.
Benefits of Taking the Test
The FLCN Gene BirtHoggDube Syndrome NGS Genetic DNA Test offers several benefits:
- Early detection of genetic mutations
- Informed decision-making regarding health management
- Guidance for family planning and risk assessment for relatives
- Access to specialized care and monitoring
Understanding Your Results
Upon completion of the test, results will be provided detailing any identified mutations in the FLCN gene. It is essential to consult with a genetic counselor to interpret these results accurately and understand their implications for your health and that of your family.
Test Pricing
| Test Name | Price (NGN) |
|---|---|
| FLCN Gene BirtHoggDube Syndrome NGS Genetic DNA Test | Discount Price: 400,000 NGN |
| Regular Price: 560,000 NGN |
Book Your Test Today!
Don’t wait for symptoms to arise. Take proactive steps towards your health by booking the FLCN Gene BirtHoggDube Syndrome NGS Genetic DNA Test today. For more information or to schedule your appointment, please call or WhatsApp us at +2348077798758.
Test Details
- 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 and a Genetic Counselling session to draw a pedigree chart of family members affected with the FLCN gene.
- Specialty: Pediatrics
- Department: Genetics
- Method: NGS Technology
- Disease Type: Dysmorphology
