PHOX2A Gene Fibrosis of Extraocular Muscles Congenital Type 2 NGS Genetic DNA Test
Introduction
The PHOX2A Gene Fibrosis of Extraocular Muscles Congenital Type 2 NGS Genetic DNA Test is a cutting-edge genetic test that plays a critical role in diagnosing congenital disorders associated with the PHOX2A gene. This test is essential for individuals who may have a genetic predisposition to extraocular muscle fibrosis, allowing for early detection and intervention.
What the Test Measures
This genetic test utilizes Next-Generation Sequencing (NGS) technology to analyze the PHOX2A gene, which is linked to conditions affecting the extraocular muscles. It detects mutations and variations that may contribute to congenital muscle fibrosis.
Who Should Consider This Test
Individuals with a family history of muscle disorders, especially those exhibiting symptoms such as strabismus (crossed eyes) or other ocular motility issues, should consider this test. Risk factors include:
- Family history of PHOX2A-related disorders
- Presence of congenital eye movement disorders
- Symptoms of ocular muscle weakness or dysfunction
Benefits of Taking the Test
Taking the PHOX2A Gene Fibrosis of Extraocular Muscles Congenital Type 2 NGS Genetic DNA Test offers several benefits:
- Accurate diagnosis of genetic conditions
- Informed decision-making for treatment options
- Early intervention and management strategies
- Genetic counseling for affected families
Understanding Your Results
Results from the PHOX2A Gene test will be interpreted by our qualified geneticists. A clear report will be provided, detailing any identified mutations and their implications. It is important to discuss these results with a healthcare provider to understand their significance and potential next steps.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| PHOX2A Gene Fibrosis of Extraocular Muscles Congenital Type 2 NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Sample Type and Turnaround Time
The test requires a sample of blood or extracted DNA, or even one drop of blood on an FTA card. The turnaround time for results is typically between 3 to 4 weeks.
Pre-Test Instructions
Before undergoing the test, patients should have a genetic counseling session to discuss their clinical history and draw a pedigree chart of family members affected by the PHOX2A gene. This information is crucial for accurate interpretation of the results.
Our Locations
DNA Labs Kenya has branches across all major cities in Kenya, ensuring accessibility for all patients. We also offer home sample collection services for your convenience.
Book Your Test Today!
Take the first step towards understanding your genetic health. Book the PHOX2A Gene Fibrosis of Extraocular Muscles Congenital Type 2 NGS Genetic DNA Test today! Call or WhatsApp us at +254711564616 for more information or to schedule your appointment.
