ALG12 Gene Glycosylation Disorder Type 1G NGS Genetic DNA Test
Introduction
The ALG12 Gene Glycosylation Disorder Type 1G NGS Genetic DNA Test is a specialized genetic test that plays a crucial role in diagnosing metabolic disorders associated with glycosylation. Understanding the genetic basis of these disorders can provide invaluable insights for patients and healthcare providers, enabling effective management and treatment strategies.
What the Test Measures
This test focuses on identifying mutations in the ALG12 gene that are responsible for Glycosylation Disorder Type 1G. By utilizing Next Generation Sequencing (NGS) technology, the test can accurately detect genetic variations that may contribute to the disorder.
Who Should Consider This Test?
Individuals who may benefit from the ALG12 Gene Glycosylation Disorder Type 1G NGS Genetic DNA Test include:
- Patients exhibiting symptoms of metabolic disorders such as developmental delays, neurological issues, or organ dysfunction.
- Family members of individuals diagnosed with Glycosylation Disorders.
- Anyone with a clinical history suggesting a glycosylation disorder.
Benefits of Taking the Test
Taking the ALG12 Gene Glycosylation Disorder Type 1G NGS Genetic DNA Test offers several benefits:
- Accurate identification of genetic mutations associated with glycosylation disorders.
- Informed decision-making regarding treatment options and family planning.
- Access to genetic counseling services for better understanding and management of the condition.
Understanding Your Results
Results from the ALG12 Gene Glycosylation Disorder Type 1G NGS Genetic DNA Test can provide critical information about the presence of genetic mutations. It is essential to discuss these results with a qualified healthcare provider who can guide you through the implications and next steps.
Test Details and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| ALG12 Gene Glycosylation Disorder Type 1G NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Test 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 Patient who is going for the test and a Genetic Counseling session to draw a pedigree chart of family members affected with Glycosylation Disorder Type 1G.
Book Your Test Today!
We have branches across Kenya, including major cities like Nairobi, Mombasa, and Kisumu. For your convenience, we also offer home sample collection services. To book the ALG12 Gene Glycosylation Disorder Type 1G NGS Genetic DNA Test, please call or WhatsApp us at +254711564616.
