PEX11B Gene Peroxisome Biogenesis Disorder 14B NGS Genetic DNA Test
Introduction to the Test
The PEX11B Gene Peroxisome Biogenesis Disorder 14B NGS Genetic DNA Test is a groundbreaking diagnostic tool that utilizes Next-Generation Sequencing (NGS) technology to identify mutations in the PEX11B gene, which are linked to peroxisome biogenesis disorders. These disorders can lead to severe neurological complications. Understanding your genetic makeup is crucial for early diagnosis and management of these conditions.
What the Test Measures
This test specifically detects mutations in the PEX11B gene, which plays a vital role in the formation and function of peroxisomes—organelles responsible for various metabolic processes in the body. By analyzing your DNA, the test can reveal the presence of genetic variations that may predispose you to neurological disorders.
Who Should Consider This Test?
Individuals who should consider the PEX11B Gene Peroxisome Biogenesis Disorder 14B NGS Genetic DNA Test include:
- Those with a family history of peroxisome biogenesis disorders.
- Patients exhibiting symptoms such as developmental delays, seizures, or neurological dysfunction.
- Individuals seeking genetic counseling for informed family planning.
Benefits of Taking the Test
- Early detection of genetic disorders, allowing for timely intervention.
- Informed decision-making regarding treatment and management options.
- Peace of mind for individuals and families regarding their genetic health.
Understanding Your Results
Results from the PEX11B Gene Peroxisome Biogenesis Disorder 14B NGS Genetic DNA Test will be interpreted by genetic specialists. A positive result may indicate a predisposition to neurological disorders, while a negative result can provide reassurance. It’s essential to discuss your results with a healthcare provider to understand their implications fully.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Book the Test
To book the PEX11B Gene Peroxisome Biogenesis Disorder 14B NGS Genetic DNA Test, please contact us at +2348110567037 or visit our website. Don’t wait—take control of your health today!
Additional Information
- Turnaround Time: 3 to 4 Weeks
- Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
- Pre-Test Instructions: Clinical history of the patient who is going for the test and a genetic counseling session to draw a pedigree chart of family members affected with PEX11B Gene Peroxisome Biogenesis Disorder 14B.
- Specialty: Neurology
- Department: Genetics
- Method: NGS Technology
- Disease Type: Neurological Disorders
