COL1A2 Gene Ehlers-Danlos Syndrome Type 7B NGS Genetic DNA Test
Introduction
The COL1A2 Gene Ehlers-Danlos Syndrome Type 7B NGS Genetic DNA Test is a vital diagnostic tool that helps in the identification of genetic predispositions to Ehlers-Danlos syndrome (EDS), particularly type 7B. EDS is a connective tissue disorder that can lead to various complications, including joint hypermobility, skin elasticity, and increased risk of injury. Understanding your genetic makeup through this test can empower patients to make informed decisions regarding their health and lifestyle.
What the Test Measures
This genetic test specifically detects mutations in the COL1A2 gene, which is essential for producing collagen, a key protein that helps maintain the structure of connective tissues. By identifying these mutations, healthcare providers can assess the risk of developing EDS type 7B.
Who Should Consider This Test
This test is recommended for individuals who exhibit symptoms of Ehlers-Danlos syndrome, such as:
- Joint hypermobility
- Skin that is easily bruised or elastic
- Family history of EDS
- Frequent joint dislocations or chronic pain
Additionally, those with a family history of COL1A2 mutations should consider this test for early detection and management.
Benefits of Taking the Test
- Early identification of genetic predispositions to EDS.
- Informed decision-making regarding health management.
- Access to tailored treatment options and lifestyle adjustments.
- Support for family planning and genetic counseling.
Understanding Your Results
Upon receiving your results, it is essential to consult with a healthcare professional to interpret the findings accurately. They will help you understand the implications of the test results and guide you on the next steps, including potential lifestyle changes or treatments.
Test Pricing
Price Type | Amount (NGN) |
---|---|
Discount Price | 400,000 NGN |
Regular Price | 560,000 NGN |
Booking the Test
To book the COL1A2 Gene Ehlers-Danlos Syndrome Type 7B NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with scheduling your appointment and answering any questions you may have.
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 the patient and a genetic counseling session to draw a pedigree chart of family members affected with COL1A2 Gene Ehlers-Danlos syndrome type 7B.
This test falls under the specialty of Dermatology, within the Genetics department, utilizing NGS technology to diagnose Osteology Dermatology Immunology Disorders.