Short Description

NGS genetic DNA test detecets for variant and mutation detection in FOXI1 gene for Deafness, autosomal recessive type 4

PreTest Information

Clinical History of Patient who is going for SLC52A3 Gene Brown-Vialetto-Van Laere syndrome 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC52A3 Gene Brown-Vialetto-Van Laere syndrome 1 NGS Genetic DNA Test gene SLC52A11

Detail Description

FOXI1 Gene Deafness: Symptoms, Diagnosis, and NGS Genetic DNA Test Cost in India

Deafness is a common condition that affects millions of people worldwide. There are many different types of deafness, and each type has its own unique causes, symptoms, and treatments. One type of deafness is caused by mutations in the FOXI1 gene, which is responsible for the development and function of the inner ear.

What is FOXI1 Gene Deafness?

FOXI1 gene deafness is a type of autosomal recessive deafness that is caused by mutations in the FOXI1 gene. This gene is responsible for the development and function of the inner ear, which is essential for hearing. When mutations occur in the FOXI1 gene, the inner ear does not develop properly, and hearing loss can occur.

Symptoms of FOXI1 Gene Deafness

The symptoms of FOXI1 gene deafness can vary depending on the severity of the mutation. Some people may have mild hearing loss, while others may be completely deaf. The symptoms of FOXI1 gene deafness may include:

• Difficulty hearing or understanding speech
• Frequent ear infections
• Trouble hearing high-pitched sounds
• Trouble hearing in noisy environments
• Balance problems

Diagnosis of FOXI1 Gene Deafness

FOXI1 gene deafness can be diagnosed through genetic testing. This involves analyzing a person's DNA to look for mutations in the FOXI1 gene. Genetic testing can be done through a blood sample or a cheek swab. If a person is found to have a mutation in the FOXI1 gene, they may be referred to an audiologist for further testing to determine the severity of their hearing loss.

NGS Genetic DNA Test Cost in India

The cost of an NGS genetic DNA test for FOXI1 gene deafness in India can vary depending on the provider. However, the average cost 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 testing.

Conclusion

FOXI1 gene deafness is a type of autosomal recessive deafness that is caused by mutations in the FOXI1 gene. The symptoms of FOXI1 gene deafness can vary, but may include difficulty hearing or understanding speech, frequent ear infections, and trouble hearing high-pitched sounds. FOXI1 gene deafness can be diagnosed through genetic testing, which can cost around INR 20,000 in India. If you suspect that you or a loved one may have FOXI1 gene deafness, it is important to speak with a healthcare provider or audiologist for further testing and treatment options.