GBA Gene Gaucher Disease Type 3 NGS Genetic DNA Test
Introduction to the Test
The GBA Gene Gaucher Disease Type 3 NGS Genetic DNA Test is a specialized genetic test that identifies mutations in the GBA gene, which are responsible for Gaucher disease type 3, a rare metabolic disorder. This test is vital for accurate diagnosis, management, and treatment planning for affected individuals and their families.
What the Test Measures
This genetic test utilizes Next Generation Sequencing (NGS) technology to detect specific mutations in the GBA gene. By analyzing a sample of blood or extracted DNA, the test identifies whether a patient carries mutations that could lead to Gaucher disease type 3.
Who Should Consider This Test?
Individuals who should consider the GBA Gene Gaucher Disease Type 3 NGS Genetic DNA Test include:
- Those with a family history of Gaucher disease or related metabolic disorders.
- Individuals presenting symptoms such as splenomegaly, bone pain, or neurological issues.
- Patients undergoing genetic counseling to understand their risk factors.
Benefits of Taking the Test
The benefits of the GBA Gene Gaucher Disease Type 3 NGS Genetic DNA Test include:
- Accurate identification of genetic mutations, aiding in early diagnosis.
- Informed decision-making regarding treatment options and family planning.
- Access to specialized care and management strategies for affected individuals.
Understanding Your Results
Results from the GBA Gene Gaucher Disease Type 3 NGS Genetic DNA Test will indicate whether mutations are present in the GBA gene. A genetic counselor will help interpret these results, providing guidance on the implications for health and family members.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| GBA Gene Gaucher Disease Type 3 NGS Genetic DNA Test | 400000 NGN | 560000 NGN |
Booking the Test
To book the GBA Gene Gaucher Disease Type 3 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.
Ensure you have a clinical history and consider a genetic counseling session to map out your family’s medical background, which is important for this test.
