Short Description

NGS genetic DNA test detecets for variant and mutation detection in LHFPL5 gene for Deafness, autosomal recessive type 67

PreTest Information

Clinical History of Patient who is going for PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test gene PTPN32

Detail Description

LHFPL5 Gene Deafness, autosomal recessive type 67 NGS Genetic DNA Test

Deafness is a condition that affects millions of people worldwide. There are various types of deafness, and one such type is autosomal recessive deafness caused by mutations in the LHFPL5 gene. This condition is also known as DFNB67. The LHFPL5 gene is responsible for encoding proteins that help in the proper functioning of the inner ear. Mutations in this gene can lead to hearing loss, which can be moderate to severe.

NGS Genetic DNA Test is a diagnostic tool that can help in identifying mutations in the LHFPL5 gene. This test uses next-generation sequencing technology to analyze DNA samples and detect any mutations that may be present in the LHFPL5 gene. The cost of the NGS Genetic DNA Test for LHFPL5 gene deafness is INR 20000.

Symptoms of LHFPL5 Gene Deafness

The symptoms of LHFPL5 gene deafness can vary from person to person. In some cases, the hearing loss may be mild, while in others, it may be severe. Some common symptoms of LHFPL5 gene deafness include:

• Difficulty in hearing high-pitched sounds
• Muffled or distorted hearing
• Difficulty in understanding speech, especially in noisy environments
• Delayed speech and language development in children
• Tinnitus or ringing in the ears

Diagnosis of LHFPL5 Gene Deafness

The diagnosis of LHFPL5 gene deafness involves a combination of tests, including:

• Hearing tests: These tests are done to determine the extent and type of hearing loss.
• Genetic testing: This involves analyzing a DNA sample to detect any mutations in the LHFPL5 gene.
• Imaging tests: These tests are done to check the structure of the inner ear and identify any abnormalities.

Conclusion

LHFPL5 gene deafness is a rare form of autosomal recessive deafness caused by mutations in the LHFPL5 gene. The NGS Genetic DNA Test is a useful diagnostic tool that can help in identifying mutations in this gene. The cost of the test is INR 20000. If you or a loved one is experiencing symptoms of hearing loss, it is essential to seek medical attention and get diagnosed as soon as possible.

At DNA Labs India, we offer a wide range of genetic testing services, including the NGS Genetic DNA Test for LHFPL5 gene deafness. Our team of experts uses state-of-the-art technology to provide accurate and reliable results. 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 LHFPL5 Gene Deafness, autosomal recessive type 67 NGS Genetic DNA Test