Short Description

NGS genetic DNA test detecets for variant and mutation detection in WFS1 gene for Wolfram-like syndrome, autosomal dominant

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 SLC52A22

Detail Description

WFS1 Gene and Wolfram-like Syndrome: Symptoms, Diagnosis, and NGS Genetic DNA Test Cost in India

Wolfram-like syndrome is a rare and inherited disorder that affects the nervous system and endocrine system of the body. It is similar to Wolfram syndrome, a genetic disorder that affects about 1 in 770,000 people worldwide. Wolfram-like syndrome is caused by mutations in the WFS1 gene, which provides instructions for making a protein called wolframin. Wolframin helps regulate the release of certain hormones and protect the body's cells from stress.

Symptoms of Wolfram-like Syndrome

Wolfram-like syndrome can cause a variety of symptoms, which can vary widely among affected individuals. Some of the most common symptoms of Wolfram-like syndrome include:

• Vision problems, including optic atrophy, which is the degeneration of the optic nerve
• Hearing loss, which can be progressive and severe
• Diabetes mellitus, which can develop in childhood or adolescence
• Urinary tract problems, including bladder dysfunction and incontinence
• Neurological problems, including seizures and ataxia
• Psychiatric problems, including depression and anxiety

Diagnosis of Wolfram-like Syndrome

Diagnosis of Wolfram-like syndrome can be challenging, as the symptoms can be similar to those of other disorders. A diagnosis is usually made based on a combination of clinical symptoms, family history, and genetic testing. Genetic testing can confirm the presence of mutations in the WFS1 gene, which are the underlying cause of the disorder.

NGS Genetic DNA Test Cost in India

NGS genetic DNA testing is a powerful tool for diagnosing genetic disorders such as Wolfram-like syndrome. NGS stands for next-generation sequencing, which is a high-throughput DNA sequencing technology that can analyze large amounts of genetic data quickly and accurately. The cost of NGS genetic DNA testing for Wolfram-like syndrome in India is approximately INR 20,000.

Conclusion

Wolfram-like syndrome is a rare and inherited disorder that affects the nervous system and endocrine system of the body. It is caused by mutations in the WFS1 gene, which provides instructions for making a protein called wolframin. Symptoms of Wolfram-like syndrome can include vision problems, hearing loss, diabetes mellitus, urinary tract problems, neurological problems, and psychiatric problems. Diagnosis is usually made based on a combination of clinical symptoms, family history, and genetic testing, including NGS genetic DNA testing, which is available in India at a cost of approximately INR 20,000.

At DNA Labs India, we offer NGS genetic DNA testing for Wolfram-like syndrome and other genetic disorders. Our testing services are accurate, reliable, and affordable, and we are committed to providing our clients with the highest level of service and support. Contact us today to learn more about our testing 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 WFS1 Gene Wolfram-like syndrome, autosomal dominant NGS Genetic DNA Test