Cox15 Gene Cardioencephalomyopathy Fatal Infantile Due to Cytochrome C Oxidase Deficiency Type 2 NGS Genetic DNA Test
Introduction
The Cox15 Gene Cardioencephalomyopathy Fatal Infantile NGS Genetic DNA Test is a cutting-edge diagnostic tool that plays a vital role in identifying cytochrome c oxidase deficiency type 2. This condition is a severe genetic disorder that can lead to fatal outcomes in infants. Early detection through this test allows for timely medical intervention, potentially improving the quality of life for affected individuals.
What the Test Measures
This genetic test analyzes the COX15 gene to detect mutations that may lead to cytochrome c oxidase deficiency. By understanding the genetic makeup of the patient, healthcare providers can assess the risk of developing this life-threatening condition.
Who Should Consider This Test
Parents with a family history of cardiomyopathy or unexplained infant fatalities should consider this test. Symptoms to watch for include:
- Unexplained lethargy in infants
- Breathing difficulties
- Growth retardation
If your child exhibits any of these symptoms or if there is a known family history of COX15-related disorders, this test is highly recommended.
Benefits of Taking the Test
- Early diagnosis of potential genetic disorders
- Informed decision-making regarding treatment options
- Access to genetic counseling and support services
- Peace of mind for families with a history of genetic conditions
Understanding Your Results
Results from the Cox15 Gene test will be provided in a comprehensive report. It is essential to consult with a genetic counselor or a specialist to interpret the findings accurately. Understanding the implications of your results can guide further medical decisions and family planning.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Cox15 Gene Cardioencephalomyopathy Fatal Infantile NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Sample Collection and Turnaround Time
The sample type required for this test can be blood, extracted DNA, or a drop of blood on an FTA card. The typical turnaround time for results is between 3 to 4 weeks.
Book Your Test Today!
We have branches across Kenya, including major cities like Nairobi, Mombasa, and Kisumu. For your convenience, we also offer home sample collection services. Don’t wait—take the first step towards understanding your health by booking the Cox15 Gene Cardioencephalomyopathy Fatal Infantile NGS Genetic DNA Test today! Call or WhatsApp us at +254711564616.
