CRYM Gene Deafness Autosomal Dominant Type 40 NGS Genetic DNA Test
Introduction
The CRYM Gene Deafness Autosomal Dominant Type 40 NGS Genetic DNA Test is a revolutionary diagnostic tool designed to identify genetic mutations associated with hearing loss. This test leverages Next Generation Sequencing (NGS) technology to provide accurate and comprehensive results. Understanding the genetic basis of deafness is crucial for effective management and treatment options, making this test invaluable for affected individuals and their families.
What the Test Measures
This genetic test specifically detects mutations in the CRYM gene, which are linked to autosomal dominant forms of deafness. By analyzing the DNA sample, our lab can determine if there are genetic variations that contribute to hearing impairment, enabling better-informed decisions regarding treatment and family planning.
Who Should Consider This Test?
Individuals with a family history of deafness, especially those who have experienced hearing loss at a young age, should consider this test. Symptoms that may indicate a need for testing include:
- Progressive hearing loss
- Sudden onset of hearing impairment
- Family members with a history of genetic hearing loss
Benefits of Taking the Test
The benefits of the CRYM Gene Deafness Autosomal Dominant Type 40 NGS Genetic DNA Test include:
- Accurate identification of genetic causes of deafness
- Informed family planning and risk assessment for future generations
- Guidance for appropriate interventions and support services
- Access to genetic counseling for better understanding and management of results
Understanding Your Results
Results from the CRYM Gene Deafness test will be provided in a clear and understandable format. Our genetic counselors will assist you in interpreting the results, discussing the implications for you and your family, and outlining potential next steps based on your findings.
Pricing Information
| Test Name | Discount Price | Regular Price |
|---|---|---|
| CRYM Gene Deafness Autosomal Dominant Type 40 NGS Genetic DNA Test | KSh 40,000 | KSh 56,000 |
Test Details
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: A clinical history of the patient is required, along with a genetic counseling session to draw a pedigree chart of family members affected by CATSPER2 Gene Deafness and male infertility.
Book Your Test Today!
We have branches across Kenya, including Nairobi, Mombasa, and Kisumu, and offer convenient home sample collection services. Don’t wait—book your CRYM Gene Deafness Autosomal Dominant Type 40 NGS Genetic DNA Test today by calling or WhatsApp us at +254711564616.
