PEX3 Gene Peroxisome Biogenesis Disorder Type 10A NGS Genetic DNA Test
Introduction
The PEX3 Gene Peroxisome Biogenesis Disorder Type 10A NGS Genetic DNA Test is a cutting-edge diagnostic tool that plays a vital role in identifying genetic mutations associated with neurological disorders. This test utilizes Next Generation Sequencing (NGS) technology, which allows for comprehensive analysis of the PEX3 gene, crucial for peroxisome function in cells.
What the Test Measures
This test specifically measures mutations in the PEX3 gene, which are linked to peroxisome biogenesis disorders. By detecting these mutations, healthcare providers can better understand the underlying genetic causes of neurological symptoms.
Who Should Consider This Test
Individuals who should consider this test include:
- Those with a family history of peroxisome biogenesis disorders.
- Patients exhibiting neurological symptoms such as developmental delays, seizures, or movement disorders.
- Individuals advised by a neurologist or genetic counselor.
Benefits of Taking the Test
- Early diagnosis of genetic disorders can lead to timely interventions.
- Understanding genetic risks can assist in family planning.
- Provides clarity on the cause of neurological symptoms.
- Guides treatment options based on genetic insights.
Understanding Your Results
Results from the PEX3 Gene test will be interpreted by a qualified genetic counselor or neurologist. They will explain whether any mutations were detected and what this means for your health and treatment options.
Test Details and Pricing
| Test Name | Price (NGN) |
|---|---|
| PEX3 Gene Peroxisome Biogenesis Disorder Type 10A NGS Genetic DNA Test |
Discount Price: 400,000 NGN Regular Price: 560,000 NGN |
Booking the Test
To book the PEX3 Gene Peroxisome Biogenesis Disorder Type 10A NGS Genetic DNA Test, please contact us via phone or WhatsApp at +2348077798758. Our team is ready to assist you with the booking process and answer any questions you may have.
Pre-Test Instructions
Before undergoing the test, it is essential to have a clinical history assessment and a genetic counseling session to draw a pedigree chart of family members affected by the PEX3 Gene Peroxisome Biogenesis Disorder Type 10A.
Sample Type
This test can be conducted using:
- Blood sample
- Extracted DNA
- One drop of blood on FTA Card
Turnaround Time
The expected turnaround time for results is between 3 to 4 weeks.
Take the first step towards understanding your genetic health today! Book your test now!
