Nx Gen Sequencing Episodic Ataxia Test
Introduction
The Nx Gen Sequencing Episodic Ataxia Test is a specialized genetic test aimed at identifying mutations related to episodic ataxia, a condition characterized by abnormal coordination and balance. This test is crucial for patients experiencing symptoms that may indicate genetic disorders affecting the nervous system. By utilizing advanced Next-Generation Sequencing (NGS) and Sanger sequencing methods, this test offers a comprehensive analysis of key genetic components associated with ataxia.
What the Test Measures
This test detects mutations in several critical genes, including:
- CACNA1A
- CACNB4
- GABRD
- GABRG2
- KCNA1
- SCN1A
- SCN1B
- SCN2A
- SCN9A
- SLC1A3
These genes are pivotal in understanding the genetic basis of episodic ataxia and other related disorders.
Who Should Consider This Test?
This test is recommended for individuals who exhibit symptoms such as:
- Unexplained balance issues
- Frequent episodes of dizziness or ataxia
- Family history of genetic disorders affecting motor functions
If you are experiencing any of these symptoms or have risk factors associated with genetic ataxia, consulting with a neurologist about this test may be beneficial.
Benefits of Taking the Test
Undergoing the Nx Gen Sequencing Episodic Ataxia Test provides several advantages:
- Accurate identification of genetic mutations
- Informed decision-making for treatment and management
- Understanding family risk factors and implications
- Access to specialized care based on genetic findings
Understanding Your Results
Results from the Nx Gen Sequencing Episodic Ataxia Test typically take about 40 working days. Once available, your healthcare provider will help interpret the findings, guiding you through the implications and potential next steps based on your genetic profile.
Test Pricing
Test Name | Discount Price | Regular Price |
---|---|---|
Nx Gen Sequencing Episodic Ataxia Test | 46800 KSh | 52000 KSh |
Sample Collection and Instructions
To conduct this test, a sample of 10 mL (5 mL min.) whole blood is required from 2 Lavender Top (EDTA) tubes. Ensure that the sample is shipped refrigerated and not frozen. A duly filled Whole Exome Sequencing Consent Form (Form 37) is mandatory for processing.
Book Your Test Today!
We have branches across all major cities in Kenya and offer home sample collection services for your convenience. To book the Nx Gen Sequencing Episodic Ataxia Test, please call or WhatsApp us at +254711564616.