CHRND Gene Myasthenic Syndrome Congenital Type 3A Slow Channel NGS Genetic DNA Test
The CHRND Gene Myasthenic Syndrome Congenital Type 3A Slow Channel NGS Genetic DNA Test is a cutting-edge diagnostic tool that utilizes next-generation sequencing (NGS) technology to identify mutations in the CHRND gene, which are associated with congenital myasthenic syndromes. This test is vital for patients experiencing muscle weakness and fatigue, providing clarity on their genetic condition and guiding treatment options.
What the Test Measures
This test specifically detects genetic variations in the CHRND gene, which plays a crucial role in neuromuscular transmission. By identifying these mutations, healthcare providers can better understand the underlying causes of muscle weakness and tailor treatment plans accordingly.
Who Should Consider This Test?
Individuals who exhibit symptoms of myasthenic syndrome, such as:
- Muscle weakness that worsens with activity
- Fatigue
- Difficulty swallowing or speaking
- Respiratory issues
are encouraged to consider this test. Additionally, those with a family history of congenital myasthenic syndromes or related neurological disorders should also seek testing.
Benefits of Taking the Test
- Early diagnosis of myasthenic syndrome, leading to timely intervention.
- Informed decision-making regarding treatment options.
- Understanding genetic risks for family members.
- Access to genetic counseling for affected families.
Understanding Your Results
Results from the CHRND Gene Myasthenic Syndrome test will help you and your healthcare provider understand the specific genetic factors at play. A genetic counseling session is recommended to interpret results and discuss implications for treatment and family planning.
Test Details and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| CHRND Gene Myasthenic Syndrome Congenital Type 3A Slow Channel NGS Genetic DNA Test | KSh 40,000 | KSh 56,000 |
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: A clinical history of the patient is required, along with a genetic counseling session to draw a pedigree chart of family members affected with CHRND Gene Myasthenic syndrome, congenital, type 3A, slow channel.
Book Your Test Today
We have branches across all major cities in Kenya, making it easy for you to access our services. To book the CHRND Gene Myasthenic Syndrome Congenital Type 3A Slow Channel NGS Genetic DNA Test, please call or WhatsApp us at +254711564616.
