CIITA Gene Bare Lymphocyte Syndrome Type 2 Complementation Group A NGS Genetic DNA Test
Introduction
The CIITA Gene Bare Lymphocyte Syndrome Type 2 Complementation Group A NGS Genetic DNA Test is a cutting-edge diagnostic tool used to identify mutations in the CIITA gene, which plays a crucial role in the immune system. Understanding these genetic factors is vital for diagnosing and managing various immunological disorders, particularly those affecting the skin and other organs.
What the Test Measures
This test measures the genetic variations in the CIITA gene, which can lead to Bare Lymphocyte Syndrome, a condition characterized by a deficiency in the immune response. It utilizes Next Generation Sequencing (NGS) technology to provide precise and comprehensive results.
Who Should Consider This Test?
Individuals who exhibit symptoms of immune dysfunction, such as recurrent infections, or those with a family history of genetic disorders affecting immunity should consider this test. Consulting with a healthcare provider can help determine if this test is appropriate based on individual health history.
Benefits of Taking the Test
- Early detection of genetic disorders that can impact health.
- Informed decision-making regarding treatment and management options.
- Understanding hereditary risks for family members.
- Access to specialized care and genetic counseling.
Understanding Your Results
Results from the CIITA Gene Bare Lymphocyte Syndrome Type 2 NGS test will provide insights into the presence of genetic mutations. A genetic counselor will help interpret these results, guiding patients through the implications for their health and potential treatment pathways.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Book Your Test Today!
To book the CIITA Gene Bare Lymphocyte Syndrome Type 2 Complementation Group A NGS Genetic DNA Test, please contact us at +2348077798758 or visit our website. Ensure your health is in good hands with DNA Labs Nigeria.
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 CIITA Gene Bare Lymphocyte Syndrome.
Specialty: Dermatology
Department: Genetics
Method: NGS Technology
Disease Type: Osteology Dermatology Immunology Disorders
