CTLA4 Gene Lymphoproliferative Syndrome Autoimmune Type 5 NGS Genetic DNA Test
Introduction to the Test
The CTLA4 Gene Lymphoproliferative Syndrome Autoimmune Type 5 NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify genetic mutations associated with autoimmune disorders stemming from the CTLA4 gene. This test is pivotal for individuals with a family history of autoimmune diseases, as it provides crucial insights into their genetic predisposition.
What the Test Measures
This genetic test utilizes Next-Generation Sequencing (NGS) technology to detect mutations in the CTLA4 gene. By analyzing the DNA from a blood sample or extracted DNA, the test can identify specific genetic variations that may lead to lymphoproliferative syndromes and other autoimmune conditions.
Who Should Consider This Test?
Individuals who exhibit symptoms such as unexplained fevers, lymphadenopathy, or recurrent infections should consider this test. Additionally, those with a family history of CTLA4-related autoimmune disorders are strongly encouraged to undergo testing to better understand their risk factors.
Benefits of Taking the Test
- Early identification of genetic predisposition to autoimmune diseases.
- Informed decision-making regarding health management and treatment options.
- Increased understanding of family health history and potential risks for relatives.
Understanding Your Results
Upon receiving your results, a healthcare professional will guide you through the findings. Positive results indicating a mutation may require further evaluation and management strategies tailored to your specific needs.
Test Pricing
Price Type | Amount (NGN) |
---|---|
Discount Price | 400,000 NGN |
Regular Price | 560,000 NGN |
Book the Test Today!
Don’t leave your health to chance. Book the CTLA4 Gene Lymphoproliferative Syndrome Autoimmune Type 5 NGS Genetic DNA Test today at DNA Labs Nigeria. For inquiries or to schedule your appointment, call or WhatsApp us at +2348077798758.
Turnaround time for results is approximately 3 to 4 weeks. Ensure to provide a clinical history and consider a genetic counseling session prior to testing to discuss your family’s health background.