DNAJC3 Gene Ataxia Combined Cerebellar and Peripheral With Hearing Loss And Diabetes Mellitus NGS Genetic DNA Test
The DNAJC3 Gene Ataxia Combined Cerebellar and Peripheral With Hearing Loss And Diabetes Mellitus NGS Genetic DNA Test is an advanced genetic analysis that plays a crucial role in diagnosing and understanding complex neurological disorders. This test is designed to detect mutations in the DNAJC3 gene, which are associated with ataxia, hearing loss, and diabetes mellitus. By using Next Generation Sequencing (NGS) technology, we can provide accurate and comprehensive insights into an individual’s genetic predisposition to these conditions.
What the Test Measures/Detects
This genetic test specifically measures the presence of mutations in the DNAJC3 gene. It evaluates the genetic factors that may lead to:
- Ataxia – a disorder affecting coordination and balance.
- Peripheral neuropathy – which can cause weakness, numbness, and pain.
- Hearing loss – which may be progressive and impact quality of life.
- Diabetes mellitus – increasing the risk of various complications.
Who Should Consider This Test
This test is recommended for individuals who exhibit symptoms or have risk factors such as:
- Family history of ataxia or neurological disorders.
- Symptoms of coordination difficulties, balance issues, or peripheral neuropathy.
- Progressive hearing loss without an apparent cause.
- Diagnosed diabetes mellitus with neurological symptoms.
Benefits of Taking the Test
Taking the DNAJC3 Gene Ataxia test offers numerous benefits, including:
- Early identification of genetic predispositions, allowing for proactive management.
- Informed family planning and genetic counseling for affected families.
- Personalized treatment options and lifestyle adjustments based on genetic findings.
- Access to support groups and resources for individuals with similar conditions.
Understanding Your Results
Results from the DNAJC3 Gene Ataxia test will provide insights into the presence or absence of mutations in the DNAJC3 gene. A genetic counselor will assist in interpreting these results, discussing implications for health management, and guiding next steps. It is essential to consider that not all genetic changes result in disease, and the significance of a mutation can vary.
Test Pricing
| Test Name | Price (NGN) |
|---|---|
| DNAJC3 Gene Ataxia Combined Cerebellar and Peripheral With Hearing Loss And Diabetes Mellitus NGS Genetic DNA Test | Discount Price: 400,000 NGN |
| Regular Price: 560,000 NGN |
Book Your Test Today!
To schedule your DNAJC3 Gene Ataxia Combined Cerebellar and Peripheral With Hearing Loss And Diabetes Mellitus NGS Genetic DNA Test, please contact us at +2348077798758 via call or WhatsApp. Our team is ready to assist you with any inquiries and help you take the first step toward understanding your genetic health.
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 DNAJC3 Gene Ataxia.
Specialty: Neurology
Department: Genetics
Method: NGS Technology
Disease Type: Neurological Disorders
