ST6GAL2 Gene Beta-Galactosamide Alpha-2,6-Sialyltransferase 2 Deficiency NGS Genetic DNA Test
Introduction
The ST6GAL2 Gene Beta-Galactosamide Alpha-2,6-Sialyltransferase 2 Deficiency NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify mutations in the ST6GAL2 gene, which plays a crucial role in the metabolism of certain sugars. This test is vital for individuals who may be at risk of metabolic disorders associated with this genetic deficiency. By utilizing Next Generation Sequencing (NGS) technology, we can provide accurate and comprehensive results that inform clinical decisions.
What the Test Measures
This genetic test measures the presence of mutations in the ST6GAL2 gene, which can lead to Beta-Galactosamide Alpha-2,6-Sialyltransferase 2 deficiency. This deficiency is associated with various metabolic disorders that can affect a person’s health and well-being.
Who Should Consider This Test
Individuals with a family history of metabolic disorders, particularly those exhibiting symptoms such as developmental delays, neurological issues, or unexplained health problems, should consider this test. Genetic counseling prior to testing is recommended to better understand the implications of the results.
Benefits of Taking the Test
- Early detection of genetic disorders.
- Informed decision-making regarding treatment options.
- Understanding potential health risks for family members.
- Access to tailored medical management strategies.
Understanding Your Results
Results from the ST6GAL2 Gene Beta-Galactosamide Alpha-2,6-Sialyltransferase 2 Deficiency NGS Genetic DNA Test will provide insight into your genetic makeup and potential risks. A genetic counselor will help interpret the results and discuss the next steps based on your individual situation.
Test Price Information
Discount Price | 400000 NGN |
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Regular Price | 560000 NGN |
Book the Test Today!
Don’t wait to understand your genetic health. Book the ST6GAL2 Gene Beta-Galactosamide Alpha-2,6-Sialyltransferase 2 Deficiency NGS Genetic DNA Test today! For more information or to schedule your appointment, call or WhatsApp us at +2348110567037.
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: A clinical history of the patient is required prior to testing, along with a genetic counseling session to draw a pedigree chart of family members affected by Beta-Galactosamide Alpha-2,6-Sialyltransferase 2 deficiency.
Specialty: General Physician
Department: Genetics
Method: NGS Technology
Disease Type: Metabolic Disorders