Short Description

NGS genetic DNA test detecets for variant and mutation detection in KARS1 gene for Deafness, autosomal recessive type 89

PreTest Information

Clinical History of Patient who is going for GJB2 Gene Deafness with keratopachydermia and constrictions of fingers and toes NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GJB2 Gene Deafness with keratopachydermia and constrictions of fingers and toes NGS Genetic DNA Test gene GJB12

Detail Description

KARS1 Gene Deafness: Symptoms, Diagnosis, and Genetic Testing Cost

Deafness is a condition that affects millions of people worldwide. It can be caused by a variety of factors, including genetic mutations. One such mutation is found in the KARS1 gene, which causes autosomal recessive type 89 deafness. In this blog, we will discuss the symptoms of KARS1 gene deafness, the diagnosis process, and the cost of genetic testing for this condition in India.

Symptoms of KARS1 Gene Deafness

KARS1 gene deafness is a rare genetic condition that affects the ability to hear. It is caused by mutations in the KARS1 gene, which provides instructions for making an enzyme called lysyl-tRNA synthetase. This enzyme is essential for the production of proteins that are important for hearing.

The symptoms of KARS1 gene deafness can vary from person to person. Some people may experience hearing loss in one ear, while others may experience hearing loss in both ears. The severity of the hearing loss can also vary, with some people experiencing mild to moderate hearing loss, while others may have profound deafness.

Other symptoms of KARS1 gene deafness can include:

• Tinnitus (ringing in the ears)
• Difficulty understanding speech, especially in noisy environments
• Difficulty hearing high-pitched sounds
• Delayed language development in children

Diagnosis of KARS1 Gene Deafness

If you or your child are experiencing symptoms of KARS1 gene deafness, it is important to see a doctor as soon as possible. Your doctor will likely refer you to an audiologist, who will perform a series of tests to determine the extent of your hearing loss.

If the audiologist suspects that your hearing loss is caused by a genetic mutation, they may recommend genetic testing. Genetic testing for KARS1 gene deafness involves analyzing a sample of your DNA to look for mutations in the KARS1 gene.

The process for genetic testing typically involves:

1. Consultation with a genetic counselor
2. Collection of a blood or saliva sample
3. Analysis of the DNA sample in a laboratory
4. Review of the results by a medical geneticist

Cost of KARS1 Gene Deafness Genetic Testing in India

The cost of genetic testing for KARS1 gene deafness can vary depending on the laboratory and the specific tests that are performed. In India, the cost of genetic testing for KARS1 gene deafness typically ranges from INR 15,000 to INR 25,000.

It is important to note that genetic testing is not always covered by insurance, so it is important to check with your insurance provider before undergoing testing. Some laboratories may also offer financial assistance or payment plans to help make testing more affordable.

Conclusion

KARS1 gene deafness is a rare genetic condition that can cause hearing loss. If you or your child are experiencing symptoms of KARS1 gene deafness, it is important to see a doctor and undergo testing as soon as possible. Genetic testing can help confirm a diagnosis and provide important information for treatment and management of the condition.

If you are interested in genetic testing for KARS1 gene deafness or other genetic conditions, contact DNA Labs India to learn more about our testing services and pricing.

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 KARS1 Gene Deafness, autosomal recessive type 89 NGS Genetic DNA Test