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Accurate Test Results for WHRN Gene Deafness, autosomal recessive type 31 NGS Genetic DNA Test
WHRN Gene Deafness, autosomal recessive type 31 NGS Genetic DNA Test Cost 20000 Rs
WHRN Gene Deafness, autosomal recessive type 31 NGS Genetic DNA Test Details
Understanding WHRN Gene Deafness - Autosomal Recessive Type 31
Deafness is a common sensory disorder that affects millions of people worldwide. It can be caused by various factors, including genetic mutations. WHRN gene deafness, also known as autosomal recessive type 31, is a genetic condition that can cause progressive hearing loss. In this blog, we will discuss the symptoms, diagnosis, and the cost of the NGS Genetic DNA test for WHRN gene deafness in India.
Symptoms of WHRN Gene Deafness
The symptoms of WHRN gene deafness can vary from person to person. Some people may experience mild hearing loss, while others may have severe deafness. The condition usually affects both ears equally and can progress over time. Some of the common symptoms of WHRN gene deafness include:
- Difficulty in hearing high-pitched sounds
- Trouble understanding speech, especially in noisy environments
- Need for increased volume on electronic devices
- Ringing in the ears (tinnitus)
- Dizziness or vertigo
Diagnosis of WHRN Gene Deafness
The diagnosis of WHRN gene deafness involves a thorough medical history and physical examination. A hearing test, known as audiometry, is usually done to measure the extent and severity of the hearing loss. In some cases, additional tests such as imaging studies or genetic testing may be required to confirm the diagnosis of WHRN gene deafness.
NGS Genetic DNA Test for WHRN Gene Deafness - Cost in India
The NGS Genetic DNA Test is a state-of-the-art diagnostic tool that can detect genetic mutations associated with WHRN gene deafness. This test uses advanced sequencing technologies to analyze the DNA of the patient and identify any mutations in the WHRN gene. The cost of the NGS Genetic DNA Test for WHRN gene deafness in India is approximately INR 20,000.
Conclusion
WHRN gene deafness is a genetic condition that can cause progressive hearing loss. It is important to recognize the symptoms of this condition and seek medical attention promptly. The NGS Genetic DNA Test is an effective diagnostic tool that can help identify the genetic mutations associated with WHRN gene deafness. If you or a loved one is experiencing hearing loss, consult a healthcare professional for a proper diagnosis and treatment.
At DNA Labs India, we offer state-of-the-art NGS Genetic DNA testing services for various genetic disorders, including WHRN gene deafness. Our team of experienced professionals uses the latest technologies and techniques 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 WHRN Gene Deafness, autosomal recessive type 31 NGS Genetic DNA Test
