COG8 Gene Glycosylation Disorder Type 2H NGS Genetic DNA Test
Introduction
The COG8 Gene Glycosylation Disorder Type 2H NGS Genetic DNA Test is a specialized genetic test that plays a vital role in diagnosing glycosylation disorders. Glycosylation disorders are a group of metabolic conditions that can lead to significant health complications. This test employs Next Generation Sequencing (NGS) technology to analyze the COG8 gene, providing insights into potential genetic mutations that may affect an individual’s health.
What the Test Measures
This test specifically measures the presence of mutations in the COG8 gene, which is crucial for proper glycosylation processes in the body. Abnormalities in this gene can lead to various metabolic disorders, impacting the body’s ability to function optimally.
Who Should Consider This Test?
Individuals who exhibit symptoms of metabolic disorders or have a family history of glycosylation disorders should consider this test. Common symptoms may include developmental delays, neurological issues, and other unexplained health problems. Additionally, those who have undergone genetic counseling or have concerns regarding inherited conditions may find this test beneficial.
Benefits of Taking the Test
- Accurate identification of genetic mutations associated with glycosylation disorders.
- Guidance for treatment options and management of symptoms.
- Informed decision-making for family planning and genetic counseling.
- Peace of mind for individuals and families regarding genetic health risks.
Understanding Your Results
Results from the COG8 Gene Glycosylation Disorder Type 2H NGS Genetic DNA Test will provide information on whether any mutations were detected. A genetic counselor or healthcare provider will help interpret the results, which can guide further medical decisions and treatment plans.
Test Information and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| COG8 Gene Glycosylation Disorder Type 2H NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Sample Type and Turnaround Time
The sample type for this test can be blood, extracted DNA, or one drop of blood on an FTA card. The turnaround time for results is approximately 3 to 4 weeks.
Pre-Test Instructions
Before undergoing the COG8 Gene Glycosylation Disorder Type 2H NGS Genetic DNA Test, it is essential to have a clinical history of the patient documented. Additionally, a genetic counseling session is recommended to draw a pedigree chart of family members affected by glycosylation disorder type 2H.
Book Your Test Today!
We have branches across major cities in Kenya, including Nairobi, Mombasa, and Kisumu, and we also offer home sample collection services. For more information or to book your test, call or WhatsApp us at +254711564616.
