CACNB4 Gene Episodic Ataxia Type 5 NGS Genetic DNA Test
Introduction
The CACNB4 Gene Episodic Ataxia Type 5 NGS Genetic DNA Test is an advanced diagnostic tool designed to identify mutations in the CACNB4 gene, which are associated with episodic ataxia type 5, a rare neurological disorder. This test utilizes Next Generation Sequencing (NGS) technology to provide a comprehensive analysis of the gene, aiding in the diagnosis and management of this condition.
What the Test Measures
This genetic test measures the presence of specific mutations in the CACNB4 gene. By analyzing the DNA, healthcare providers can determine if a patient is genetically predisposed to episodic ataxia type 5, allowing for tailored treatment plans and interventions.
Who Should Consider This Test?
Individuals experiencing symptoms such as:
- Unexplained episodes of balance problems
- Sudden dizziness or vertigo
- Coordination difficulties
- Family history of neurological disorders
should consider undergoing this test. Additionally, those with risk factors related to neurological disorders may benefit from genetic counseling and testing.
Benefits of Taking the Test
- Identifies genetic predispositions to episodic ataxia type 5.
- Aids in understanding the underlying causes of neurological symptoms.
- Informs treatment options and management strategies.
- Facilitates family planning and genetic counseling.
Understanding Your Results
Results from the CACNB4 Gene Episodic Ataxia Type 5 NGS Genetic DNA Test will indicate whether mutations are present. A positive result may suggest a genetic predisposition to the disorder, while a negative result may provide reassurance. It is essential to discuss your results with a qualified healthcare provider, who can guide you through the implications and next steps.
Test Pricing
Test Name | Discount Price (NGN) | Regular Price (NGN) |
---|---|---|
CACNB4 Gene Episodic Ataxia Type 5 NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Call to Action
To book the CACNB4 Gene Episodic Ataxia Type 5 NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you in understanding your genetic health and ensuring you receive the best possible care.
Additional Information
Turnaround time for the results is approximately 3 to 4 weeks. The sample type required for this test can be blood, extracted DNA, or one drop of blood on an FTA card. Prior to testing, a clinical history and a genetic counseling session to create a pedigree chart of affected family members are recommended.
Consult with a neurologist for further evaluation and guidance on your health concerns related to neurological disorders.