PEX1 Gene Peroxisome Biogenesis Disorder Type 1B NGS Genetic DNA Test
Introduction
The PEX1 Gene Peroxisome Biogenesis Disorder Type 1B NGS Genetic DNA Test is an advanced diagnostic tool designed to identify mutations in the PEX1 gene, which are associated with peroxisome biogenesis disorders. These disorders are a group of rare genetic conditions that can lead to severe neurological complications. Understanding your genetic makeup is crucial for early diagnosis, intervention, and management of these conditions.
What the Test Measures
This genetic test utilizes Next Generation Sequencing (NGS) technology to analyze the PEX1 gene. It detects specific mutations that can lead to peroxisome biogenesis disorder type 1B, providing insights into a patient’s genetic predisposition to neurological disorders.
Who Should Consider This Test?
This test is recommended for individuals who:
- Have a family history of peroxisome biogenesis disorders.
- Exhibit symptoms such as developmental delays, seizures, or neurological issues.
- Wish to understand their genetic risk factors for neurological disorders.
Benefits of Taking the Test
Taking the PEX1 Gene test offers several benefits:
- Early identification of genetic disorders for timely intervention.
- Informed family planning and risk assessment.
- Access to tailored treatment options and management strategies.
Understanding Your Results
Results from the PEX1 Gene test will be provided with a detailed explanation. It is essential to consult with a healthcare professional or a genetic counselor to interpret the results accurately and discuss the implications for you and your family.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| PEX1 Gene Peroxisome Biogenesis Disorder Type 1B NGS Genetic DNA Test | KSh 40,000 | KSh 56,000 |
Sample Type and Turnaround Time
The test requires a sample of either blood or extracted DNA, or even one drop of blood on an FTA card. The expected turnaround time for results is approximately 3 to 4 weeks.
Pre-Test Instructions
Before undergoing the PEX1 Gene test, it is essential to have a clinical history assessment and a genetic counseling session. This session will help in drawing a pedigree chart of family members affected by the disorder, which is crucial for accurate interpretation of results.
Branches Across Kenya
We have branches in all major cities in Kenya, making it easy for you to access our services. Additionally, we offer a home sample collection service for your convenience.
Book Your Test Today!
Don’t wait for symptoms to appear. Book the PEX1 Gene Peroxisome Biogenesis Disorder Type 1B NGS Genetic DNA Test today by calling or WhatsApping us at +254711564616. Take the first step towards understanding your health!
