Short Description

NGS genetic DNA test detecets for variant and mutation detection in SERPINB6 gene for Deafness, autosomal recessive type 91

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 SLC52A14

Detail Description

SERPINB6 Gene Deafness: Symptoms, Diagnosis, and NGS Genetic DNA Test Cost

Deafness is a common condition that affects millions of people worldwide. It can be caused by various factors, including genetics. One of the genes that have been associated with deafness is the SERPINB6 gene. This gene is responsible for the production of a protein called SCCA1, which is involved in the regulation of cell growth and differentiation. Mutations in the SERPINB6 gene can lead to deafness, autosomal recessive type 91.

Symptoms of SERPINB6 Gene Deafness

The symptoms of SERPINB6 gene deafness can vary depending on the severity of the condition. Some of the common symptoms include:

• Hearing loss
• Tinnitus (ringing in the ears)
• Difficulty understanding speech
• Difficulty hearing in noisy environments

The symptoms usually appear in early childhood and can progressively worsen over time.

Diagnosis of SERPINB6 Gene Deafness

Diagnosis of SERPINB6 gene deafness involves a combination of physical examination, hearing tests, and genetic testing. A doctor may examine the ear canal and eardrum to determine the extent of hearing loss. Hearing tests may include pure-tone audiometry, speech audiometry, and otoacoustic emissions testing.

Genetic testing can confirm whether the patient has a mutation in the SERPINB6 gene. This can be done through Next-Generation Sequencing (NGS) genetic testing, which is a state-of-the-art technology that can sequence large amounts of DNA quickly and accurately. NGS genetic testing can identify mutations in multiple genes associated with deafness, including the SERPINB6 gene.

NGS Genetic DNA Test Cost

The cost of NGS genetic DNA testing for SERPINB6 gene deafness in India is around INR 20,000. This may vary depending on the testing laboratory and the specific tests that are performed. However, the cost of genetic testing can be a worthwhile investment for patients and their families, as it can provide valuable information about the cause of deafness and help guide treatment and management strategies.

Conclusion

SERPINB6 gene deafness is a rare but significant cause of hearing loss, particularly in childhood. Symptoms can vary, but may include hearing loss, tinnitus, and difficulty understanding speech. Diagnosis involves physical examination, hearing tests, and genetic testing, including NGS genetic DNA testing. The cost of NGS genetic DNA testing for SERPINB6 gene deafness in India is around INR 20,000. Early diagnosis and intervention can help improve outcomes for patients and their families.

If you suspect that you or a loved one may have SERPINB6 gene deafness, it's important to speak with a healthcare provider and consider genetic testing.

At DNA Labs India, we offer a wide range of genetic testing services, including NGS genetic DNA testing for SERPINB6 gene deafness. Our team of experts can provide personalized guidance and support throughout the testing process. Contact us today to learn more.

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 SERPINB6 Gene Deafness, autosomal recessive type 91 NGS Genetic DNA Test