FGFR2 Gene Jackson-Weiss Syndrome NGS Genetic DNA Test
Introduction
The FGFR2 Gene Jackson-Weiss Syndrome NGS Genetic DNA Test is a revolutionary diagnostic tool designed to identify mutations in the FGFR2 gene, which are associated with Jackson-Weiss syndrome. This genetic condition is characterized by specific craniofacial anomalies and skeletal dysplasia. Early diagnosis through this test is crucial for managing symptoms and providing appropriate care.
What the Test Measures
This test utilizes Next-Generation Sequencing (NGS) technology to analyze the FGFR2 gene for any pathogenic variants. By detecting these mutations, healthcare providers can better understand the genetic predisposition of individuals to Jackson-Weiss syndrome.
Who Should Consider This Test?
Individuals who exhibit symptoms of Jackson-Weiss syndrome or have a family history of dysmorphology should consider this test. Symptoms may include:
- Craniofacial abnormalities
- Foot deformities
- Other skeletal anomalies
Additionally, those with risk factors such as family history or previous diagnoses of related conditions are encouraged to undergo testing.
Benefits of Taking the Test
- Early detection of genetic disorders
- Informed decision-making regarding treatment and management
- Understanding the risk of recurrence in future pregnancies
- Access to genetic counseling and support
Understanding Your Results
Results from the FGFR2 Gene Jackson-Weiss Syndrome NGS Genetic DNA Test will provide insights into the presence of FGFR2 mutations. A genetic counselor will assist in interpreting these results, explaining their implications and the next steps in care.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400000 NGN |
| Regular Price | 560000 NGN |
Book the Test
To schedule your FGFR2 Gene Jackson-Weiss Syndrome NGS Genetic DNA Test, please contact us at +2348077798758 or visit our website to book your appointment today. Take the first step towards understanding your genetic health!
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: A clinical history of the patient is required, along with a genetic counseling session to create a pedigree chart of family members affected by FGFR2 mutations.
This test falls under the specialty of Pediatrics, within the Genetics department, focusing on dysmorphology through advanced NGS technology.
