ALG11 Gene Congenital Disorder of Glycosylation Type Ip NGS Genetic DNA Test
The ALG11 Gene Congenital Disorder of Glycosylation Type Ip NGS Genetic DNA Test is a cutting-edge genetic test designed to identify mutations in the ALG11 gene that can lead to metabolic disorders. This test is vital for accurate diagnosis and management of congenital disorders of glycosylation, which can significantly impact a patient’s health and quality of life.
What the Test Measures
This test specifically measures genetic variations in the ALG11 gene. These variations can disrupt normal glycosylation processes in the body, leading to a range of metabolic disorders. By identifying these mutations, healthcare providers can better understand the underlying causes of symptoms and tailor treatment plans accordingly.
Who Should Consider This Test?
Individuals who should consider the ALG11 Gene Test include:
- Patients exhibiting symptoms of metabolic disorders, such as developmental delays or neurological issues.
- Individuals with a family history of congenital disorders of glycosylation.
- Patients who have undergone previous genetic testing that indicated potential glycosylation issues.
Benefits of Taking the Test
Taking the ALG11 Gene Congenital Disorder of Glycosylation Type Ip NGS Genetic DNA Test offers several benefits:
- Accurate identification of genetic mutations that may be causing health issues.
- Informed decisions regarding treatment and management plans.
- Opportunity for genetic counseling and understanding family health risks.
- Access to advanced NGS technology for precise results.
Understanding Your Results
Results from the ALG11 Gene Test will typically be ready within 3 to 4 weeks. Once received, healthcare providers will interpret the results and discuss their implications with the patient. It is important to understand that a positive result indicates the presence of a mutation, while a negative result does not rule out the possibility of other metabolic disorders.
Pricing Information
| Test Name | Discount Price | Regular Price |
|---|---|---|
| ALG11 Gene Congenital Disorder of Glycosylation Type Ip NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Sample Collection and Pre-Test Instructions
Sample types accepted for this test include:
– Blood
– Extracted DNA
– One drop of blood on an FTA card
Prior to testing, a clinical history must be provided, and a genetic counseling session is recommended to draw a pedigree chart of family members affected by congenital disorders of glycosylation, type Ip.
Book Your Test Today
We have branches across all major cities in Kenya, making it easy for you to access our services. For your convenience, we also offer home sample collection services. Book the test today or call/WhatsApp us at +254711564616!
