SLC35A2 Gene Glycosylation Disorder Type 2M NGS Genetic DNA Test
Introduction
The SLC35A2 Gene Glycosylation Disorder Type 2M NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify mutations in the SLC35A2 gene, which are associated with glycosylation disorders. These disorders can lead to a range of metabolic issues, making early detection crucial for effective management and treatment.
What Does the Test Measure?
This test utilizes Next Generation Sequencing (NGS) technology to detect specific genetic variations in the SLC35A2 gene. By analyzing the genetic material, the test can identify mutations that may lead to abnormal glycosylation, a process essential for proper cellular function.
Who Should Consider This Test?
Individuals with a family history of glycosylation disorders or those showing symptoms such as developmental delays, neurological issues, or metabolic irregularities should consider this test. Additionally, those with risk factors for metabolic disorders may benefit from early genetic testing.
Benefits of Taking the Test
- Early identification of genetic predispositions to glycosylation disorders.
- Informed decision-making regarding treatment and management options.
- Potential for personalized medicine based on genetic findings.
- Peace of mind for families with a history of metabolic disorders.
Understanding Your Results
Results from the SLC35A2 Gene Glycosylation Disorder Type 2M NGS Genetic DNA Test will be interpreted by our qualified genetic counselors. They will guide you through the implications of your results and discuss any necessary follow-up actions or treatments.
Test Information
| Test Name | Discount Price | Regular Price |
|---|---|---|
| SLC35A2 Gene Glycosylation Disorder Type 2M NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking Your Test
To book the SLC35A2 Gene Glycosylation Disorder Type 2M NGS Genetic DNA Test, please contact us at +2348077798758 or visit our website. Ensure you have a clinical history and consider a genetic counseling session to draw a pedigree chart of family members affected by Glycosylation Disorder Type 2M.
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-test Instructions: Clinical history of the patient is required.
