COMP Gene Pseudoachondroplasia NGS Genetic DNA Test
Introduction
The COMP Gene Pseudoachondroplasia NGS Genetic DNA Test is a cutting-edge diagnostic tool that utilizes Next Generation Sequencing (NGS) technology to analyze the COMP gene. This test is crucial for identifying pseudoachondroplasia, a genetic disorder that impacts bone growth and development. Understanding genetic predispositions is vital for effective management and counseling for affected individuals and their families.
What the Test Measures
This test specifically measures mutations in the COMP gene, which is responsible for the production of cartilage oligomeric matrix protein. Abnormalities in this gene can lead to pseudoachondroplasia, characterized by disproportionate short stature and skeletal abnormalities.
Who Should Consider This Test?
Individuals who exhibit symptoms such as disproportionate short stature, joint pain, or have a family history of pseudoachondroplasia should consider this test. It is also recommended for those who have undergone genetic counseling and wish to understand their genetic risks better.
Benefits of Taking the Test
- Accurate diagnosis of pseudoachondroplasia through genetic analysis.
- Informed family planning and management options.
- Access to tailored medical care and interventions based on genetic findings.
- Empowerment through understanding genetic health risks.
Understanding Your Results
Results from the COMP Gene Pseudoachondroplasia NGS Genetic DNA Test will provide insights into the presence of mutations in the COMP gene. A genetic counselor will assist in interpreting these results, discussing implications for health, family planning, and potential treatment options.
Test Pricing
Test Name | Discount Price | Regular Price |
---|---|---|
COMP Gene Pseudoachondroplasia NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book Your Test
Take the first step towards understanding your genetic health by booking the COMP Gene Pseudoachondroplasia NGS Genetic DNA Test today! For inquiries or to schedule your appointment, please call or WhatsApp us at +2348077798758.
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 prior to the test. It is recommended to have a genetic counseling session to draw a pedigree chart of family members affected by the COMP gene.
Specialty: Dermatology
Department: Genetics
Method: NGS Technology
Disease Type: Osteology, Dermatology, Immunology Disorders