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Accurate Test Results for POU4F3 Gene Deafness, autosomal dominant type 15 NGS Genetic DNA Test
POU4F3 Gene Deafness, autosomal dominant type 15 NGS Genetic DNA Test Cost 20000 Rs
POU4F3 Gene Deafness, autosomal dominant type 15 NGS Genetic DNA Test Details
POU4F3 Gene Deafness, Autosomal Dominant Type 15 NGS Genetic DNA Test Cost - DNA Labs India
Deafness is a condition where a person is unable to hear sounds. It can be caused by various factors such as genetics, infections, exposure to loud noises, and certain medications. In this blog, we will discuss POU4F3 gene deafness, autosomal dominant type 15 NGS genetic DNA test cost, symptoms, and diagnosis at DNA Labs India.
POU4F3 Gene Deafness, Autosomal Dominant Type 15
POU4F3 gene deafness, autosomal dominant type 15 is a genetic disorder that affects the inner ear. It is caused by mutations in the POU4F3 gene, which provides instructions for making a protein called Brn-3c. This protein is essential for the normal development and function of hair cells in the inner ear, which are responsible for converting sound waves into electrical signals that are sent to the brain.
When the POU4F3 gene is mutated, the hair cells in the inner ear do not function properly, leading to hearing loss. The severity of hearing loss can vary from mild to profound, and it can affect one or both ears. This condition is inherited in an autosomal dominant pattern, which means that a person only needs to inherit one copy of the mutated gene from either parent to develop the condition.
NGS Genetic DNA Test for POU4F3 Gene Deafness, Autosomal Dominant Type 15
NGS genetic DNA test is a type of genetic test that analyzes the DNA sequence of a person to identify mutations in specific genes. It is a highly accurate and sensitive test that can detect even small changes in the DNA sequence. DNA Labs India offers NGS genetic DNA test for POU4F3 gene deafness, autosomal dominant type 15.
The cost of the NGS genetic DNA test for POU4F3 gene deafness, autosomal dominant type 15 at DNA Labs India is INR 20,000. The test requires a blood sample from the person being tested, which is analyzed in the laboratory to identify any mutations in the POU4F3 gene. The results of the test can help in the diagnosis of the condition and can also be used for genetic counseling.
Symptoms of POU4F3 Gene Deafness, Autosomal Dominant Type 15
The symptoms of POU4F3 gene deafness, autosomal dominant type 15 can vary from person to person and can range from mild to severe. The most common symptom is hearing loss, which can be either progressive or sudden. Other symptoms may include:
- Tinnitus (ringing in the ears)
- Difficulty hearing in noisy environments
- Difficulty hearing high-pitched sounds
- Balance problems
- Dizziness
Diagnosis of POU4F3 Gene Deafness, Autosomal Dominant Type 15
The diagnosis of POU4F3 gene deafness, autosomal dominant type 15 is based on the symptoms, family history, and genetic testing. A person with a family history of the condition and who exhibits symptoms of hearing loss should undergo genetic testing to confirm the diagnosis.
NGS genetic DNA test is the most accurate and sensitive test for the diagnosis of POU4F3 gene deafness, autosomal dominant type 15. The test can identify any mutations in the POU4F3 gene and can confirm the diagnosis.
Conclusion
POU4F3 gene deafness, autosomal dominant type 15 is a genetic disorder that affects the inner ear and can lead to hearing loss. NGS genetic DNA test is a highly accurate and sensitive test that can detect mutations in the POU4F3 gene and can help in the diagnosis of the condition. DNA Labs India offers NGS genetic DNA test for POU4F3 gene deafness, autosomal dominant type 15 at a cost of INR 20,000. If you or someone in your family is exhibiting symptoms of hearing loss, it is important to undergo genetic testing to confirm the diagnosis and to receive appropriate treatment and genetic counseling.
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 POU4F3 Gene Deafness, autosomal dominant type 15 NGS Genetic DNA Test
