LHFPL5 Gene Deafness Autosomal Recessive Type 67 NGS Genetic DNA Test
Introduction
The LHFPL5 Gene Deafness Autosomal Recessive Type 67 NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify genetic mutations associated with hereditary deafness. This test employs Next-Generation Sequencing (NGS) technology to analyze the LHFPL5 gene, which plays a crucial role in hearing function. Understanding genetic predispositions can significantly impact early diagnosis and management of hearing disorders.
What the Test Measures
This genetic test specifically detects mutations in the LHFPL5 gene that are linked to autosomal recessive deafness. By analyzing the DNA extracted from a blood sample or a drop of blood on an FTA card, the test provides insights into the genetic factors contributing to hearing loss.
Who Should Consider This Test?
Individuals with a family history of hearing loss, especially those exhibiting symptoms such as late-onset deafness or unexplained hearing impairment, should consider this test. Additionally, those with risk factors such as a known genetic disorder in the family or congenital hearing loss should seek testing to understand their genetic risks.
Benefits of Taking the Test
- Early identification of genetic causes of hearing loss.
- Informed decision-making regarding family planning.
- Access to targeted interventions and management strategies.
- Contribution to personalized healthcare approaches.
Understanding Your Results
Results from the LHFPL5 Gene Deafness Autosomal Recessive Type 67 NGS Genetic DNA Test will provide information on whether mutations are present in the LHFPL5 gene. A genetic counseling session is recommended to help interpret the results accurately and discuss potential implications for family members.
Test Pricing
Test Name | Discount Price | Regular Price |
---|---|---|
LHFPL5 Gene Deafness Autosomal Recessive Type 67 NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Branches and Booking
We have branches across all major cities in Kenya, making it convenient for you to access our services. For those unable to visit, we offer home sample collection services. Don’t wait to understand your genetic health—book your test today! Call or WhatsApp us at +254746849631.
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: Clinical History of Patient who is going for PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test gene PTPN32
Specialty: ENT Doctor | Department: Genetics | Method: NGS Technology | Disease Type: Ear Nose Throat Disorders