Short Description

NGS genetic DNA test detecets for variant and mutation detection in CISD2 gene for Wolfram syndrome type 2

PreTest Information

Clinical History of Patient who is going for EYA1 Gene Branchiootic syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with EYA1 Gene Branchiootic syndrome type 1 NGS Genetic DNA Test gene EYA20

Detail Description

CISD2 Gene Wolfram Syndrome Type 2 NGS Genetic DNA Test Cost INR:20,000 Symptoms Diagnosis

Introduction

Wolfram syndrome type 2 is a rare genetic disorder that affects the nervous system and can lead to hearing loss, vision loss, diabetes, and other health problems. The CISD2 gene is one of the genes associated with this condition. A NGS genetic DNA test can help diagnose this condition and determine if an individual is a carrier for the mutation. In this blog, we will discuss the symptoms, diagnosis, and cost of the CISD2 gene Wolfram syndrome type 2 NGS genetic DNA test in India.

Symptoms of Wolfram Syndrome Type 2

The symptoms of Wolfram syndrome type 2 typically appear in childhood or adolescence and can include:

• Hearing loss
• Vision loss
• Diabetes
• Bladder and bowel problems
• Depression and anxiety
• Difficulty with balance and coordination

Diagnosis of Wolfram Syndrome Type 2

A diagnosis of Wolfram syndrome type 2 is typically made based on the presence of symptoms and genetic testing. A NGS genetic DNA test can detect mutations in the CISD2 gene that are associated with this condition. This test can also determine if an individual is a carrier for the mutation.

CISD2 Gene Wolfram Syndrome Type 2 NGS Genetic DNA Test Cost

The cost of the CISD2 gene Wolfram syndrome type 2 NGS genetic DNA test in India is approximately INR 20,000. This cost may vary depending on the testing facility and location.

Conclusion

Wolfram syndrome type 2 is a rare genetic disorder that can have serious health consequences. The CISD2 gene is one of the genes associated with this condition, and a NGS genetic DNA test can help diagnose this condition and determine if an individual is a carrier for the mutation. If you or a loved one is experiencing symptoms of Wolfram syndrome type 2, it is important to speak with a healthcare provider and consider genetic testing.