CRYAB Gene Myopathy Desmin Related Associated With Mutation In The CRYAB Gene NGS Genetic DNA Test
Introduction to the CRYAB Gene Myopathy NGS Genetic DNA Test
The CRYAB Gene Myopathy NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify mutations in the CRYAB gene, which are associated with various neurological disorders. Understanding these genetic mutations is vital for accurate diagnosis and effective treatment planning. This test employs Next-Generation Sequencing (NGS) technology, ensuring high sensitivity and specificity in detecting genetic anomalies.
What the Test Measures
This test focuses on detecting mutations in the CRYAB gene, which is linked to desmin-related myopathy. By analyzing the genetic material, it helps identify specific changes that may contribute to muscle and neurological dysfunction.
Who Should Consider This Test?
Individuals experiencing symptoms such as muscle weakness, difficulty in movement, or family history of neurological disorders should consider this test. Additionally, those with risk factors for genetic myopathies may benefit from this comprehensive analysis.
Benefits of Taking the Test
- Accurate diagnosis of CRYAB gene mutations.
- Informed treatment decisions based on genetic insights.
- Potential for early intervention in progressive conditions.
- Guidance for family planning through genetic counseling.
Understanding Your Results
Results from the CRYAB Gene Myopathy NGS Genetic DNA Test will provide insights into the presence of genetic mutations. A healthcare professional will assist in interpreting these results and discussing potential implications for treatment and management.
Test Pricing
| Price Type | Amount (KSh) |
|---|---|
| Discount Price | 40,000 |
| Regular Price | 56,000 |
Book Your Test Today!
We have branches across all major cities in Kenya, including Nairobi, Mombasa, and Kisumu. Our team is ready to assist you with the CRYAB Gene Myopathy NGS Genetic DNA Test. For home sample collection and further inquiries, please call or WhatsApp us at +254711564616.
Test Details
- Turnaround Time: 3 to 4 Weeks
- Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
- Pre-Test Instructions: Clinical history of the patient and a genetic counseling session to draw a pedigree chart of affected family members.
- Specialty: Neurology
- Department: Genetics
- Method: NGS Technology
- Disease Type: Neurological Disorders
