SCO2 Gene Cardioencephalomyopathy Fatal Infantile Due to Cytochrome C Oxidase Deficiency NGS Genetic DNA Test
Introduction
The SCO2 Gene Cardioencephalomyopathy Fatal Infantile NGS Genetic DNA Test is a vital diagnostic tool that helps in identifying cytochrome c oxidase deficiency, a rare but severe genetic disorder that can lead to fatal outcomes in infants. Early detection through this test is crucial for implementing timely medical interventions, thus improving the chances of better health outcomes for affected children.
What the Test Measures
This genetic test analyzes the SCO2 gene, which plays a significant role in mitochondrial function. It detects mutations that may lead to cytochrome c oxidase deficiency, a condition that affects energy production in cells, particularly in the heart and brain.
Who Should Consider This Test
This test is recommended for:
- Infants showing symptoms of cardiomyopathy, such as difficulty breathing, fatigue, or poor feeding.
- Families with a history of genetic disorders related to mitochondrial dysfunction.
- Infants diagnosed with unexplained neurological or cardiovascular issues.
Benefits of Taking the Test
Undergoing the SCO2 Gene Cardioencephalomyopathy test offers several benefits:
- Early diagnosis of potential genetic disorders.
- Informed decision-making for parents regarding treatment options.
- Access to specialized care and genetic counseling.
- Better management of symptoms and potential complications.
Understanding Your Results
Results from the SCO2 Gene test will be provided with an interpretation guide. A positive result indicates the presence of mutations in the SCO2 gene, while a negative result suggests no identified mutations. It is essential to discuss results with a healthcare provider for appropriate follow-up and management.
Test Price
| Discount Price | Regular Price |
|---|---|
| 400000 NGN | 560000 NGN |
Booking Your Test
To ensure the health and well-being of your child, consider booking the SCO2 Gene Cardioencephalomyopathy Fatal Infantile NGS Genetic DNA Test today. For more information or to schedule your test, please call or WhatsApp us at +2348077798758.
Pre-Test Instructions
Before the test, it is essential to provide a clinical history of the patient. Additionally, a genetic counseling session is recommended to draw a pedigree chart of family members affected by this condition.
Test Details
Turnaround Time: 3 to 4 weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Ensure your child’s health by taking this proactive step with the SCO2 Gene Cardioencephalomyopathy Fatal Infantile NGS Genetic DNA Test.
