DPM1 Gene Glycosylation Disorder Type 1E NGS Genetic DNA Test
Introduction
The DPM1 Gene Glycosylation Disorder Type 1E NGS Genetic DNA Test is a cutting-edge diagnostic tool that utilizes Next-Generation Sequencing (NGS) technology to identify genetic mutations associated with glycosylation disorders. These disorders can lead to various metabolic complications, making early detection crucial for effective management and treatment.
What the Test Measures
This test specifically measures variations in the DPM1 gene, which plays a vital role in the glycosylation process—an essential biochemical modification that affects protein function and stability. By analyzing the DNA, healthcare providers can understand if a patient has a predisposition to glycosylation disorder type 1E.
Who Should Consider This Test
Individuals who exhibit symptoms of metabolic disorders, such as developmental delays, neurological issues, or abnormal organ function, should consider this test. Additionally, those with a family history of glycosylation disorders or related metabolic conditions are encouraged to undergo testing for a comprehensive understanding of their genetic health.
Benefits of Taking the Test
- Early diagnosis of potential metabolic disorders.
- Informed decision-making regarding health management.
- Personalized treatment plans based on genetic findings.
- Peace of mind for individuals and families with a history of glycosylation disorders.
Understanding Your Results
Results from the DPM1 Gene Glycosylation Disorder Type 1E NGS Genetic DNA Test provide valuable insights into your genetic predisposition. A genetic counseling session is recommended to discuss results, draw a pedigree chart, and understand the implications for family members.
Test Information and Pricing
Test Name | Discount Price (NGN) | Regular Price (NGN) |
---|---|---|
DPM1 Gene Glycosylation Disorder Type 1E NGS Genetic DNA Test | 400,000 | 560,000 |
How to Book the Test
To take the first step towards understanding your genetic health, book the DPM1 Gene Glycosylation Disorder Type 1E NGS Genetic DNA Test today! Call or WhatsApp us at +2348077798758 for more information and to schedule your appointment.
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 clinical history of the patient is required, along with a genetic counseling session to draw a pedigree chart of family members affected by glycosylation disorder type 1E.
Specialty: General Physician
Department: Genetics
Method: NGS Technology
Disease Type: Metabolic Disorders