ALG6 Gene Glycosylation Disorder Type 1C NGS Genetic DNA Test
Introduction
The ALG6 Gene Glycosylation Disorder Type 1C NGS Genetic DNA Test is a cutting-edge diagnostic tool that utilizes Next Generation Sequencing (NGS) technology to identify mutations in the ALG6 gene. This test is crucial for understanding glycosylation disorders, which can lead to significant neurological complications. Early detection through this genetic test allows for timely intervention and management of associated symptoms.
What the Test Measures
This genetic test detects specific mutations in the ALG6 gene that are responsible for glycosylation disorders. By analyzing the DNA sample, the test can reveal whether an individual has inherited a mutation that could lead to neurological disorders.
Who Should Consider This Test
This test is recommended for individuals who:
- Have a family history of glycosylation disorders or neurological conditions.
- Exhibit symptoms such as developmental delays, seizures, or other neurological issues.
- Are seeking genetic counseling to understand their risk or that of their offspring.
Benefits of Taking the Test
- Early identification of genetic mutations linked to neurological disorders.
- Informed decision-making regarding treatment options.
- Ability to provide tailored care and management strategies.
- Support for family planning through genetic counseling.
Understanding Your Results
Results from the ALG6 Gene Glycosylation Disorder Type 1C NGS Genetic DNA Test will indicate whether any mutations were detected. A genetic counselor or healthcare professional will help interpret these results, providing guidance on potential next steps based on your specific situation.
Test Information and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| ALG6 Gene Glycosylation Disorder Type 1C NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Additional Information
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Turnaround Time: 3 to 4 Weeks
Pre-test Instructions: A clinical history of the patient going for the ALG6 Gene Glycosylation Disorder Type 1C NGS Genetic DNA Test is required. A genetic counseling session to draw a pedigree chart of family members affected with ALG6 Gene Glycosylation Disorder Type 1C is also recommended.
Book Your Test Today!
We have branches across Kenya, making it convenient for you to access our services. For more information or to book your test, please call or WhatsApp us at +254711564616. Don’t wait—take the first step towards understanding your health today!
