Myo1A Gene Deafness Autosomal Dominant Type 48 NGS Genetic DNA Test
Introduction
The Myo1A Gene Deafness Autosomal Dominant Type 48 NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify genetic mutations associated with hereditary hearing loss. This test plays a crucial role in understanding the genetic basis of deafness, allowing healthcare providers to offer personalized management plans for affected individuals and their families.
What the Test Measures
This genetic test specifically analyzes the Myo1A gene, which has been linked to autosomal dominant forms of hearing impairment. By using Next Generation Sequencing (NGS) technology, the test can detect mutations that may lead to progressive or profound hearing loss.
Who Should Consider This Test
Individuals who should consider the Myo1A Gene Deafness Test include:
- Those with a family history of hearing loss.
- Individuals experiencing unexplained hearing impairment.
- Patients referred by an ENT specialist for genetic evaluation.
Benefits of Taking the Test
Taking the Myo1A Gene Deafness Test offers several advantages:
- Early diagnosis of genetic hearing loss.
- Informed decision-making regarding treatment options.
- Guidance for family planning and understanding inheritance patterns.
- Access to genetic counseling and support services.
Understanding Your Results
Upon receiving your results, a genetic counselor will help interpret the findings. Results may indicate the presence of mutations in the Myo1A gene, which can inform your healthcare provider about the potential implications for your hearing health and that of your family members.
Test Pricing
Test Name | Discount Price | Regular Price |
---|---|---|
Myo1A Gene Deafness Autosomal Dominant Type 48 NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Branches and Booking
We have branches across all major cities in Kenya, providing convenient access to our services. You can also opt for home sample collection. To book the Myo1A Gene Deafness Autosomal Dominant Type 48 NGS Genetic DNA Test, please call or WhatsApp us at +254711564616. Ensure you have a clinical history prepared, and consider a genetic counseling session to discuss family implications.