Short Description

NGS genetic DNA test detecets for variant and mutation detection in GRHL2 gene for Deafness, autosomal dominant type 28

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 PTPN25

Detail Description

GRHL2 Gene Deafness - DNA Labs India

GRHL2 Gene Deafness, autosomal dominant type 28 is a rare genetic condition that affects the ability to hear. It is caused by mutations in the GRHL2 gene, which provides instructions for making a protein that is important for the development and maintenance of the inner ear.

NGS Genetic DNA Test cost

At DNA Labs India, the cost of NGS Genetic DNA Test for GRHL2 Gene Deafness, autosomal dominant type 28 is INR 20,000.

Symptoms

The symptoms of GRHL2 Gene Deafness, autosomal dominant type 28 may vary from person to person. Some common symptoms include:

• Hearing loss
• Tinnitus (ringing in the ears)
• Difficulty understanding speech, especially in noisy environments
• Balance problems

Diagnosis

Diagnosis of GRHL2 Gene Deafness, autosomal dominant type 28 involves a comprehensive evaluation of the patient's medical history, physical examination, and hearing tests. Genetic testing may also be recommended to confirm the diagnosis and identify the specific mutation in the GRHL2 gene.

Conclusion

GRHL2 Gene Deafness, autosomal dominant type 28 is a rare genetic condition that affects the ability to hear. At DNA Labs India, we offer NGS Genetic DNA Test for this condition at an affordable cost of INR 20,000. If you are experiencing symptoms of hearing loss, tinnitus, or balance problems, we recommend seeking medical attention and genetic testing to confirm a diagnosis.

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 GRHL2 Gene Deafness, autosomal dominant type 28 NGS Genetic DNA Test