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 analyze genetic mutations associated with glycosylation disorders. These disorders can lead to a variety of neurological complications, making early detection and intervention crucial. This test employs Next Generation Sequencing (NGS) technology, providing a comprehensive analysis of the DPM1 gene, which plays a vital role in glycosylation processes in the body.
What the Test Measures
This genetic test detects mutations in the DPM1 gene that are responsible for Glycosylation Disorder Type 1E. By identifying these mutations, healthcare providers can better understand the genetic basis of neurological symptoms and formulate more effective treatment plans.
Who Should Consider This Test?
This test is recommended for individuals who exhibit symptoms of neurological disorders or have a family history of such conditions. Key symptoms may include:
- Developmental delays
- Neurological deficits
- Intellectual disabilities
- Seizures
If you or a family member is experiencing these symptoms, it is advisable to consult a healthcare professional about the benefits of this test.
Benefits of Taking the Test
- Early diagnosis of glycosylation disorders
- Informed treatment decisions based on genetic insights
- Family planning guidance through genetic counseling
- Access to specialized care for managing symptoms
Understanding Your Results
After the test is completed, results will be interpreted by a qualified geneticist or neurologist. They will provide insights into the presence of any mutations, their implications for health, and potential treatment options. It is important to discuss the results in the context of your overall health and family history.
Test Pricing
Test Name | Discount Price | Regular Price |
---|---|---|
DPM1 Gene Glycosylation Disorder Type 1E NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Additional Information
Turnaround time for results is typically 3 to 4 weeks. The sample type required can be blood, extracted DNA, or one drop of blood on an FTA card. Prior to testing, a clinical history and a genetic counseling session to draw a pedigree chart of affected family members are recommended.
Book Your Test Today!
At DNA Labs Kenya, we have branches across major cities including Nairobi, Mombasa, and Kisumu. We also offer home sample collection services for your convenience. To schedule your DPM1 Gene Glycosylation Disorder Type 1E NGS Genetic DNA Test, please call or WhatsApp us at +254711564616.