DPM1 Gene Glycosylation Disorder Type 1E NGS Genetic DNA Test
Introduction
The DPM1 Gene Glycosylation Disorder Type 1E NGS Genetic DNA Test is a specialized diagnostic tool designed to identify mutations in the DPM1 gene, which can lead to glycosylation disorders affecting neurological function. This test utilizes Next Generation Sequencing (NGS) technology, providing a comprehensive analysis of the genetic material to detect potential abnormalities. Understanding your genetic health is crucial in managing and preventing associated health issues.
What the Test Measures
This genetic test measures the presence of mutations in the DPM1 gene, which is responsible for the proper glycosylation of proteins. Glycosylation is a vital process that affects protein function, and disruptions can lead to severe neurological disorders.
Who Should Consider This Test?
Individuals who exhibit symptoms of glycosylation disorders, such as developmental delays, seizures, or other neurological symptoms, should consider this test. Additionally, those with a family history of these conditions may benefit from genetic testing to assess their risk and guide family planning.
Benefits of Taking the Test
- Early diagnosis of potential neurological disorders.
- Informed decision-making regarding treatment options.
- Understanding familial risks and implications for family members.
- Access to genetic counseling for better management of health.
Understanding Your Results
Results from the DPM1 Gene Glycosylation Disorder Type 1E NGS Genetic DNA Test will provide insights into the presence of any mutations. A genetic counselor will help interpret these results, discuss their implications, and guide you on the next steps for management or treatment.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Booking the Test
To book the DPM1 Gene Glycosylation Disorder Type 1E NGS Genetic DNA Test, please contact us at +2348077798758 or visit our website. Ensure you have a clinical history ready, and consider a genetic counseling session to discuss your family’s health background prior to testing.
Additional Information
- Turnaround Time: 3 to 4 Weeks
- Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
- Specialty: Neurology
- Department: Genetics
- Method: NGS Technology
- Disease Type: Neurological Disorders
