Short Description

NGS genetic DNA test detecets for variant and mutation detection in LRTOMT gene for Deafness, autosomal recessive type 63

PreTest Information

Clinical History of Patient who is going for SLC52A2 Gene Brown-Vialetto-Van Laere syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC52A2 Gene Brown-Vialetto-Van Laere syndrome type 2 NGS Genetic DNA Test gene SLC52A11

Detail Description

LRTOMT Gene Deafness, Autosomal Recessive Type 63 NGS Genetic DNA Test Cost INR: 20000 Symptoms Diagnosis

Deafness is a common condition that affects millions of people around the world. It can be caused by a variety of factors, including genetics. LRTOMT gene deafness is an autosomal recessive type of deafness that affects individuals with mutations in the LRTOMT gene. This type of deafness is also known as DFNB63 and is caused by mutations in the LRTOMT gene located on chromosome 11.

Symptoms of LRTOMT Gene Deafness

The symptoms of LRTOMT gene deafness can vary from person to person. Some individuals may experience mild to moderate hearing loss, while others may experience severe or profound hearing loss. The hearing loss may be present from birth or may develop over time. Other symptoms may include:

• Tinnitus (ringing in the ears)
• Difficulty understanding speech
• Difficulty hearing in noisy environments
• Difficulty hearing high-pitched sounds

Diagnosis of LRTOMT Gene Deafness

Diagnosis of LRTOMT gene deafness is done through genetic testing. Next-generation sequencing (NGS) genetic DNA testing is the most commonly used method for diagnosing this condition. NGS is a high-throughput method that can analyze large amounts of DNA in a short period of time. The test can detect mutations in the LRTOMT gene that are associated with DFNB63. The cost of the NGS genetic DNA test for LRTOMT gene deafness is INR 20,000.

Conclusion

LRTOMT gene deafness is an autosomal recessive type of deafness that is caused by mutations in the LRTOMT gene. The symptoms of this condition can vary from person to person, and diagnosis is done through genetic testing. NGS genetic DNA testing is the most commonly used method for diagnosing this condition, and the cost of the test is INR 20,000. If you or someone you know is experiencing symptoms of LRTOMT gene deafness, it is important to seek medical attention and get a proper diagnosis.

At DNA Labs India, we offer NGS genetic DNA testing for LRTOMT gene deafness and other genetic conditions. Our team of experts is dedicated to providing accurate and reliable genetic testing services to our clients. Contact us today to learn more about our services and how we can help you.

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 LRTOMT Gene Deafness, autosomal recessive type 63 NGS Genetic DNA Test