ADAMTS2 Gene Ehlers-Danlos Syndrome Type 7C NGS Genetic DNA Test
Introduction
The ADAMTS2 Gene Ehlers-Danlos Syndrome Type 7C NGS Genetic DNA Test is a state-of-the-art diagnostic tool designed to identify mutations in the ADAMTS2 gene. This gene is pivotal in the production of collagen, a vital protein that ensures the integrity of connective tissues. Understanding the genetic basis of Ehlers-Danlos syndrome type 7C is crucial for accurate diagnosis and management of this hereditary condition.
What the Test Measures
This genetic test specifically detects mutations in the ADAMTS2 gene. By analyzing the DNA extracted from a blood sample, the test can confirm or rule out the presence of genetic variants associated with Ehlers-Danlos syndrome type 7C.
Who Should Consider This Test
Individuals showing symptoms of connective tissue disorders, such as hypermobility, skin elasticity, and joint instability, should consider this test. Family history of Ehlers-Danlos syndrome or related conditions may also warrant genetic testing to assess risk factors.
Benefits of Taking the Test
- Provides a definitive diagnosis for Ehlers-Danlos syndrome type 7C.
- Guides treatment and management strategies for affected individuals.
- Offers valuable information for family planning and genetic counseling.
- Helps in understanding the severity and implications of the condition.
Understanding Your Results
Results from the ADAMTS2 Gene Ehlers-Danlos Syndrome Type 7C NGS Genetic DNA Test will be reviewed by your healthcare provider. They will explain the findings, including whether a mutation was detected and what that means for your health and management options.
Test Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| ADAMTS2 Gene Ehlers-Danlos Syndrome Type 7C NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book Your Test Today!
Don’t wait to gain clarity on your genetic health. To book the ADAMTS2 Gene Ehlers-Danlos Syndrome Type 7C NGS Genetic DNA Test, please call or WhatsApp us at +2348110567037. Our team is ready to assist you with any questions and to guide you through the process.
Additional Information
Turnaround time for results is approximately 3 to 4 weeks. A blood sample is required for this test. Prior to testing, a clinical history and genetic counseling session are recommended to discuss family history and to draw a pedigree chart of affected family members.
This test falls under the specialty of Dermatology and the department of Genetics, utilizing NGS Technology to provide accurate results for Osteology, Dermatology, and Immunology Disorders.
