Alg13 Gene Glycosylation Disorder Type 1S NGS Genetic DNA Test
Introduction to the Test
The Alg13 Gene Glycosylation Disorder Type 1S NGS Genetic DNA Test is a sophisticated diagnostic tool that plays a crucial role in identifying metabolic disorders caused by glycosylation abnormalities. Utilizing Next Generation Sequencing (NGS) technology, this test offers detailed insights into genetic variations that may lead to significant health issues.
What the Test Measures
This genetic test specifically detects mutations in the ALG13 gene, which is vital for proper glycosylation processes in the body. By analyzing the genetic code, the test can identify potential disruptions that may contribute to metabolic disorders.
Who Should Consider This Test?
Individuals experiencing symptoms related to glycosylation disorders, such as developmental delays, neurological issues, or unexplained metabolic problems, should consider this test. Additionally, those with a family history of metabolic disorders may benefit from genetic testing to assess their risk.
Benefits of Taking the Test
- Provides clarity on genetic conditions affecting health.
- Guides treatment options and management strategies.
- Helps in family planning by identifying hereditary risks.
- Offers peace of mind through accurate diagnosis.
Understanding Your Results
Results from the Alg13 Gene Glycosylation Disorder Type 1S NGS Genetic DNA Test will be provided in a comprehensive report. It is essential to consult with a healthcare professional to interpret the results accurately and discuss potential next steps.
Test Pricing
Test Name | Discount Price | Regular Price |
---|---|---|
Alg13 Gene Glycosylation Disorder Type 1S NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Branches and Booking
We have branches across Kenya, including major cities such as Nairobi, Mombasa, and Kisumu. Our services include home sample collection for your convenience. To book the Alg13 Gene Glycosylation Disorder Type 1S NGS Genetic DNA Test, please call or WhatsApp us at +254711564616.
Pre-Test Instructions
Before taking the test, patients are advised to undergo a genetic counseling session to discuss clinical history and draw a pedigree chart of family members affected by Glycosylation Disorder Type 1S.
Turnaround Time
The expected turnaround time for results is approximately 3 to 4 weeks.
Sample Type
The test can be conducted using a blood sample, extracted DNA, or even a single drop of blood on an FTA card.