SLC35C1 Gene Glycosylation Disorder Type 2C NGS Genetic DNA Test
Introduction
The SLC35C1 Gene Glycosylation Disorder Type 2C NGS Genetic DNA Test is a specialized diagnostic tool designed to identify genetic mutations associated with glycosylation disorders. Glycosylation is a critical biochemical process that affects how proteins are formed and function in the body. Disorders in this pathway can lead to a range of metabolic issues, making early detection essential for managing health outcomes.
What the Test Measures
This test utilizes Next-Generation Sequencing (NGS) technology to analyze the SLC35C1 gene, detecting any mutations that may disrupt normal glycosylation processes. By identifying these mutations, healthcare providers can better understand a patient’s genetic predisposition to glycosylation disorders.
Who Should Consider This Test?
Individuals who may benefit from this test include:
- Those with a family history of glycosylation disorders.
- Patients exhibiting symptoms related to metabolic disorders, such as developmental delays or organ dysfunction.
- Individuals seeking genetic counseling for family planning.
Benefits of Taking the Test
- Early detection of potential genetic disorders.
- Informed decision-making regarding treatment and management options.
- Guidance for family members about their genetic risks.
Understanding Your Results
Results from the SLC35C1 Gene Glycosylation Disorder Type 2C NGS Genetic DNA Test typically take 3 to 4 weeks. A genetic counselor will help interpret the results, explaining any identified mutations and their implications for your health and that of your family.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| SLC35C1 Gene Glycosylation Disorder Type 2C NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book Your Test Today!
To ensure your health and well-being, consider booking the SLC35C1 Gene Glycosylation Disorder Type 2C NGS Genetic DNA Test at DNA Labs Nigeria. For more information or to schedule your appointment, please call or WhatsApp us at +2348110567037.
Pre-test instructions include a clinical history assessment and a genetic counseling session to draw a pedigree chart of family members affected by glycosylation disorder type 2C. The sample type required for this test can be blood, extracted DNA, or one drop of blood on an FTA card.
