TRIP11 Gene Achondrogenesis Type 1A NGS Genetic DNA Test
Introduction to the Test
The TRIP11 Gene Achondrogenesis Type 1A NGS Genetic DNA Test is a specialized genetic test designed to detect mutations in the TRIP11 gene, which are associated with Achondrogenesis type 1A. This condition is characterized by severe skeletal abnormalities and is often identified in prenatal screenings. Understanding the genetic factors involved is crucial for informed medical decisions and family planning.
What the Test Measures
This test utilizes Next Generation Sequencing (NGS) technology to analyze the TRIP11 gene. By identifying specific mutations, healthcare providers can assess the risk of Achondrogenesis type 1A in individuals and their offspring.
Who Should Consider This Test?
Individuals or couples who have:
- A family history of Achondrogenesis type 1A
- Symptoms suggestive of skeletal abnormalities
- Risk factors associated with genetic conditions
This test is particularly recommended for prospective parents seeking to understand their genetic risks before conception.
Benefits of Taking the Test
- Provides clarity on genetic risks associated with Achondrogenesis type 1A.
- Informs family planning decisions.
- Guides healthcare professionals in managing potential health issues.
- Offers peace of mind to families concerned about genetic conditions.
Understanding Your Results
Results from the TRIP11 Gene Achondrogenesis Type 1A NGS Genetic DNA Test will indicate whether mutations are present in the TRIP11 gene. A genetic counseling session is recommended to help interpret the results and discuss potential implications for family planning and health management.
Test Information and Pricing
Test Name | Discount Price | Regular Price |
---|---|---|
TRIP11 Gene Achondrogenesis Type 1A NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking the Test
To book the TRIP11 Gene Achondrogenesis Type 1A NGS Genetic DNA Test, please contact us at +2348110567037. Our team is ready to assist you with any questions and guide you through the booking process.
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 and a Genetic Counseling session to draw a pedigree chart of family members affected with TRIP11 Gene Achondrogenesis type 1A.
This test falls under the specialty of Dermatology and the department of Genetics, addressing Osteology, Dermatology, and Immunology Disorders.