Deafness, a condition that significantly impacts an individual’s quality of life, can stem from various causes, including genetic factors. One such genetic condition is the LHFPL5 gene deafness autosomal recessive type 67. Understanding the symptoms and the availability of genetic testing for this condition is crucial for early detection and management. DNA Labs UAE offers a comprehensive genetic test for this condition, priced at 4400 AED, providing a valuable resource for affected individuals and their families.
Symptoms of LHFPL5 Gene Deafness Autosomal Recessive Type 67
The LHFPL5 gene is pivotal in the development and function of hair cells in the inner ear, which are essential for normal hearing. Mutations in this gene lead to a form of hearing loss that is inherited in an autosomal recessive pattern, meaning that an individual must inherit two copies of the mutated gene, one from each parent, to be affected. The symptoms of this condition typically manifest as follows:
- Prelingual Non-Syndromic Hearing Loss: Individuals with this condition often experience severe to profound hearing loss from birth or before they acquire speech (prelingual).
- Progressive Hearing Loss: While the hearing loss is primarily present from an early age, it may progressively worsen over time.
- High Frequencies Affected: The hearing loss predominantly affects high frequencies, though low frequencies can also be impacted as the condition progresses.
- Absence of Other Symptoms: This type of hearing loss is non-syndromic, meaning it occurs without other signs or symptoms.
Early detection through genetic testing is vital for managing the condition effectively. It allows for timely interventions, such as hearing aids, cochlear implants, and other supportive measures, to improve communication abilities and quality of life.
Genetic Test for LHFPL5 Gene Deafness Autosomal Recessive Type 67
DNA Labs UAE offers a genetic test specifically designed to diagnose mutations in the LHFPL5 gene associated with deafness autosomal recessive type 67. The test is priced at 4400 AED and involves a simple, non-invasive procedure. By analyzing an individual’s DNA, the test can confirm the presence of the specific genetic mutations responsible for this condition, providing a definitive diagnosis.
This genetic test is particularly recommended for individuals who have a family history of hearing loss or who have children showing signs of hearing impairment at an early age. Early diagnosis through genetic testing can significantly impact the management and outcome of the condition, enabling personalized treatment plans and support for affected individuals and their families.
For more information on the LHFPL5 gene deafness autosomal recessive type 67 genetic test, including how to arrange for testing, please visit DNA Labs UAE.
Understanding the genetic basis of hearing loss can empower affected individuals and their families with the knowledge and resources needed to tackle this challenge. With advancements in genetic testing, such as the test offered by DNA Labs UAE, early diagnosis and intervention are more accessible than ever, offering hope and support to those affected by genetic forms of deafness.
