Short Description

NGS genetic DNA test detecets for variant and mutation detection in SLC17A8 gene for Deafness, autosomal dominant type 25

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 IARS4

Detail Description

SLC17A8 Gene Deafness: Symptoms, Diagnosis, and NGS Genetic DNA Test Cost in India

Deafness is a common genetic disorder that affects millions of people worldwide. It is caused by mutations in several genes that are responsible for the development and function of the inner ear. One such gene is SLC17A8, which is associated with autosomal dominant type 25 deafness. In this blog, we will discuss the symptoms, diagnosis, and cost of NGS genetic DNA test for SLC17A8 gene deafness in India.

What is SLC17A8 Gene Deafness?

SLC17A8 gene deafness is a rare genetic disorder that affects the inner ear and causes progressive hearing loss. It is an autosomal dominant type of deafness, which means that a person only needs to inherit one mutated gene from either parent to develop the condition. The SLC17A8 gene provides instructions for the production of a protein called vesicular glutamate transporter 3 (VGLUT3), which is essential for the transmission of sound signals from the inner ear to the brain.

Symptoms of SLC17A8 Gene Deafness

The symptoms of SLC17A8 gene deafness usually appear in childhood or early adulthood and worsen over time. The severity of hearing loss can vary from mild to profound and may affect one or both ears. Some common symptoms of SLC17A8 gene deafness include:

• Difficulty hearing high-frequency sounds
• Trouble understanding speech, especially in noisy environments
• Frequent ear infections
• Tinnitus (ringing in the ears)
• Balance problems

Diagnosis of SLC17A8 Gene Deafness

SLC17A8 gene deafness can be diagnosed through genetic testing, which involves analyzing a person's DNA to detect mutations in the SLC17A8 gene. The most common type of genetic testing used for SLC17A8 gene deafness is Next-Generation Sequencing (NGS), which can detect mutations in multiple genes simultaneously. Other diagnostic tests for SLC17A8 gene deafness may include hearing tests, imaging tests, and physical examinations.

NGS Genetic DNA Test Cost for SLC17A8 Gene Deafness in India

The cost of NGS genetic DNA test for SLC17A8 gene deafness in India may vary depending on the laboratory and location. On average, the cost of NGS genetic DNA test for SLC17A8 gene deafness in India is around INR 20,000. However, some laboratories may offer discounts or special packages for genetic testing.

Conclusion

SLC17A8 gene deafness is a rare genetic disorder that affects the inner ear and causes progressive hearing loss. It can be diagnosed through genetic testing, especially NGS genetic DNA test, which can detect mutations in the SLC17A8 gene. The cost of NGS genetic DNA test for SLC17A8 gene deafness in India may vary depending on the laboratory and location. If you or someone you know is experiencing symptoms of SLC17A8 gene deafness, it is important to seek medical attention and genetic 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 SLC17A8 Gene Deafness, autosomal dominant type 25 NGS Genetic DNA Test