EPB42 Gene Spherocytosis Type 5 NGS Genetic DNA Test
Introduction
The EPB42 Gene Spherocytosis Type 5 NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify mutations in the EPB42 gene, which are responsible for hereditary spherocytosis. This condition leads to the destruction of red blood cells, resulting in anemia and other serious health issues. Understanding your genetic predisposition is crucial for effective management and treatment.
What the Test Measures
This comprehensive genetic test uses Next Generation Sequencing (NGS) technology to analyze the EPB42 gene. It detects mutations that may contribute to the development of hereditary spherocytosis, providing essential information for diagnosis and treatment planning.
Who Should Consider This Test?
Individuals with a family history of hematological disorders, particularly those experiencing symptoms such as:
- Fatigue
- Jaundice
- Enlarged spleen
- Frequent infections
If you have risk factors associated with hereditary spherocytosis, this test is highly recommended.
Benefits of Taking the Test
- Early diagnosis of hereditary spherocytosis.
- Informed decisions regarding treatment options.
- Family planning and genetic counseling insights.
- Peace of mind through understanding genetic health.
Understanding Your Results
Results from the EPB42 Gene Spherocytosis Type 5 NGS Genetic DNA Test will provide insight into whether you carry mutations associated with the condition. A genetic counseling session is recommended to help interpret the results and discuss potential implications for you and your family.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| EPB42 Gene Spherocytosis Type 5 NGS Genetic DNA Test | KSh 40,000 | KSh 56,000 |
Branches and Booking
We have branches across Kenya, including major cities like Nairobi, Mombasa, and Kisumu. We also offer home sample collection services for your convenience. To book the EPB42 Gene Spherocytosis Type 5 NGS Genetic DNA Test, please call or WhatsApp us at +254711564616.
Pre-Test Instructions
Before undergoing the test, please ensure you have a clinical history of the patient and consider a genetic counseling session to draw a pedigree chart of family members affected by the EPB42 gene.
