Short Description

NGS genetic DNA test detecets for variant and mutation detection in OTOA gene for Deafness, autosomal recessive type 22

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 IARS8

Detail Description

OTOA Gene Deafness: Symptoms, Diagnosis, and NGS Genetic DNA Test Cost in India

Deafness is a condition that affects millions of people worldwide, and it can be caused by genetic factors. One of these genetic factors is OTOA gene deafness, which is an autosomal recessive type 22 (DFNB22) disorder. In this blog, we will discuss the symptoms of OTOA gene deafness, how it is diagnosed, and the cost of NGS genetic DNA testing for this disorder in India.

What is OTOA Gene Deafness?

The OTOA gene is responsible for providing instructions for making a protein that is essential for the normal development and function of the inner ear. Mutations in this gene can lead to OTOA gene deafness, which is an inherited condition that affects the ability to hear. This type of deafness is autosomal recessive, which means that a person must inherit two copies of the mutated gene (one from each parent) to develop the condition.

Symptoms of OTOA Gene Deafness

The symptoms of OTOA gene deafness can vary from person to person, but they typically include:

• Difficulty hearing sounds at normal volumes
• Trouble understanding speech, especially in noisy environments
• Frequent ear infections
• Tinnitus (ringing in the ears)
• Vertigo (dizziness)

These symptoms can begin at any age, but they are usually present at birth or early childhood. In some cases, the symptoms may not become noticeable until later in life.

Diagnosis of OTOA Gene Deafness

The diagnosis of OTOA gene deafness typically involves a combination of hearing tests and genetic testing. A hearing test, also known as an audiogram, can help determine the severity and type of hearing loss. Genetic testing can confirm the presence of mutations in the OTOA gene.

NGS genetic DNA testing is a type of genetic testing that can sequence multiple genes at once, making it a more efficient and cost-effective way to diagnose genetic disorders like OTOA gene deafness.

NGS Genetic DNA Test Cost in India

The cost of NGS genetic DNA testing for OTOA gene deafness in India can vary depending on the laboratory and the specific tests performed. However, on average, the cost of this test is around INR 20,000.

It is important to note that genetic testing is not always covered by insurance, so it is important to check with your provider before undergoing any testing.

Conclusion

OTOA gene deafness is a rare genetic disorder that can lead to hearing loss. The symptoms of this condition can vary, but they typically include difficulty hearing sounds at normal volumes, trouble understanding speech, and frequent ear infections. Diagnosis of OTOA gene deafness typically involves a combination of hearing tests and genetic testing, including NGS genetic DNA testing. The cost of this test in India is around INR 20,000.

If you suspect that you or a loved one may have OTOA gene deafness, it is important to seek medical attention and undergo testing as soon as possible.

Before getting tested ask for Raw Data, FASTQ, and VCF files along with clinical test report from DNA Testing Lab. DNA Labs India is the Only lab that is transparent and will share Raw Data, FASTQ, and VCF files along with the conclusive clinical report for OTOA Gene Deafness, autosomal recessive type 22 NGS Genetic DNA Test