CACNA1A Gene Episodic Ataxia Type 2 NGS Genetic DNA Test
Introduction
The CACNA1A Gene Episodic Ataxia Type 2 NGS Genetic DNA Test is a specialized genetic test that plays a pivotal role in diagnosing episodic ataxia type 2, a neurological disorder caused by mutations in the CACNA1A gene. This test utilizes Next Generation Sequencing (NGS) technology to provide an in-depth analysis of the genetic material, allowing for precise identification of mutations that may lead to this disorder.
What the Test Measures
This test measures the presence of mutations in the CACNA1A gene, which is responsible for encoding a calcium channel that is crucial for normal neuronal function. By detecting these mutations, healthcare providers can assess the risk of developing episodic ataxia type 2 and related neurological disorders.
Who Should Consider This Test
Individuals who experience symptoms such as recurrent episodes of loss of coordination, dizziness, or balance issues, particularly those with a family history of neurological disorders, should consider this test. Additionally, those who have been diagnosed with episodic ataxia type 2 may benefit from this test to understand the genetic underpinnings of their condition.
Benefits of Taking the Test
- Early detection of genetic predisposition to episodic ataxia type 2.
- Informed decision-making regarding treatment and management options.
- Guidance for family planning and genetic counseling.
- Access to tailored therapeutic interventions based on genetic findings.
Understanding Your Results
Results from the CACNA1A Gene Episodic Ataxia Type 2 NGS Genetic DNA Test are typically available within 3 to 4 weeks. A positive result indicates the presence of a mutation associated with the disorder, while a negative result suggests that no such mutation was detected. It is important to discuss your results with a healthcare professional, preferably a neurologist or genetic counselor, to understand the implications fully.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| CACNA1A Gene Episodic Ataxia Type 2 NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book the Test
To book your CACNA1A Gene Episodic Ataxia Type 2 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.
Pre-Test Instructions
Prior to taking the test, it is essential to have a clinical history reviewed by a healthcare professional. A genetic counseling session is recommended to create a pedigree chart of family members affected by CACNA1A Gene Episodic Ataxia Type 2.
For further inquiries or to schedule your test, don’t hesitate to reach out to us!
