Short Description

NGS genetic DNA test detecets for variant and mutation detection in CIB2 gene for Deafness, autosomal recessive type 48

PreTest Information

Clinical History of Patient who is going for IARS2 Gene Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with IARS2 Gene Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia NGS Genetic DNA Test gene IARS10

Detail Description

CIB2 Gene Deafness: Autosomal Recessive Type 48 NGS Genetic DNA Test Cost INR 20,000

Deafness is a common problem that affects millions of people worldwide. There are different types of deafness, and they can be caused by various factors. One of the most common types of deafness is autosomal recessive deafness. This type of deafness is caused by genetic mutations that affect the function of the inner ear. One gene that has been linked to autosomal recessive deafness is the CIB2 gene. The CIB2 gene provides instructions for making a protein that is important for the development and function of hair cells in the inner ear. Hair cells are responsible for converting sound waves into electrical signals that are sent to the brain. Mutations in the CIB2 gene can lead to the loss of hair cells and, consequently, hearing loss. If you suspect that you or your child may have CIB2 gene deafness, it is essential to get a proper diagnosis. One way to do this is by undergoing an NGS genetic DNA test. NGS stands for Next-Generation Sequencing, which is a modern and highly accurate method for analyzing DNA. At DNA Labs India, we offer an NGS genetic DNA test for CIB2 gene deafness. This test costs INR 20,000 and involves analyzing your DNA to identify any mutations in the CIB2 gene. The test is non-invasive, and all we need is a small sample of your saliva or blood. Symptoms of CIB2 Gene Deafness The symptoms of CIB2 gene deafness can vary depending on the severity of the mutation. Some people may experience mild hearing loss, while others may be completely deaf. Symptoms may include: - Difficulty hearing in noisy environments - Trouble understanding speech - Difficulty hearing high-pitched sounds - Needing to turn up the volume on the TV or radio - Ringing in the ears (tinnitus) - Feeling like sounds are muffled or distorted Diagnosis of CIB2 Gene Deafness Diagnosing CIB2 gene deafness involves a series of tests and evaluations. The first step is usually a hearing test, which can determine the severity and type of hearing loss. If the hearing test indicates that there may be a genetic cause for the hearing loss, an NGS genetic DNA test can be performed to identify any mutations in the CIB2 gene. If you or your child has been diagnosed with CIB2 gene deafness, it is essential to seek medical care. There are various treatments and assistive devices that can help manage the symptoms of hearing loss. Conclusion CIB2 gene deafness is a type of autosomal recessive deafness caused by mutations in the CIB2 gene. If you suspect that you or your child may have this condition, it is essential to seek a proper diagnosis. At DNA Labs India, we offer an NGS genetic DNA test for CIB2 gene deafness, which costs INR 20,000. The test is non-invasive and highly accurate, and it can help identify any mutations in the CIB2 gene that may be causing hearing loss. If you have any questions or would like to schedule a test, please contact us.