The ALG11 Gene Congenital Disorder of Glycosylation Type Ip NGS Genetic DNA Test is crucial for diagnosing metabolic disorders. Priced at 40000 KSh, this test employs advanced NGS technology to provide accurate results. Ideal for patients with specific symptoms or family histories of congenital disorders. Available across Kenya with home sample collection options.
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ALG11 Gene Congenital Disorder of Glycosylation Type Ip Genetic Test
Genetic Testing
ALG11 Gene Congenital Disorder of Glycosylation Type Ip Genetic Test
KSh 56,000.00
Regular price
KSh 47,600.00
Current price
-15%
What Is the ALG11 Gene Congenital Disorder of Glycosylation Type Ip Genetic 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.
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.
What Does the Test Detect or Measure?
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.
Sample Requirements
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.
What the Results May Show
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.
Benefits or Clinical Value
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.
Pricing
| Test Name | Current Price | Regular Price |
|---|---|---|
| ALG11 Gene Congenital Disorder of Glycosylation Type Ip Genetic Test | KSh 47,600.00 | KSh 56,000.00 |
Book the ALG11 Gene Congenital Disorder of Glycosylation Type Ip Genetic Test
Contact Biopassion Diagnostics to confirm sample requirements and schedule this test.
SKU: 4f11b55f5761 | Category: Genetic Testing