DNMT1 Gene Cerebellar Ataxia with Deafness and Narcolepsy Autosomal Recessive NGS Genetic DNA Test
Introduction
The DNMT1 Gene Cerebellar Ataxia with Deafness and Narcolepsy Autosomal Recessive NGS Genetic DNA Test is a specialized genetic test that analyzes the DNMT1 gene to determine if mutations are present that could lead to significant neurological disorders. This test is essential for individuals with a family history of these conditions, allowing for early diagnosis and potential intervention.
What the Test Measures
This test uses Next Generation Sequencing (NGS) technology to detect mutations in the DNMT1 gene. These mutations are associated with a combination of cerebellar ataxia, deafness, and narcolepsy, which can severely impact an individual’s quality of life.
Who Should Consider This Test?
Individuals who exhibit symptoms such as:
- Unexplained balance issues or coordination problems
- Hearing loss
- Excessive daytime sleepiness or sudden sleep attacks
Additionally, those with a family history of neurological disorders, particularly related to the DNMT1 gene, should consider this test to assess their risk and guide management strategies.
Benefits of Taking the Test
- Early detection of genetic conditions, allowing for timely interventions.
- Informed family planning and management options based on genetic insights.
- Access to specialized care and resources for affected individuals.
Understanding Your Results
Results from the DNMT1 Gene Cerebellar Ataxia with Deafness and Narcolepsy test will provide insights into whether a mutation is present. A genetic counseling session is recommended to help interpret the results and discuss potential next steps.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Booking Information
To book the DNMT1 Gene Cerebellar Ataxia with Deafness and Narcolepsy Autosomal Recessive NGS Genetic DNA Test, please call or WhatsApp us at +2348077798758. Our team is ready to assist you with the booking process and answer any questions you may have.
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: A Genetic Counselling session to draw a pedigree chart of family members affected with DNMT1 Gene Cerebellar Ataxia with Deafness and Narcolepsy is required.
Consult with a Neurologist or a genetic specialist for more personalized insights regarding this test and its implications for your health.
