Short Description

NGS genetic DNA test detecets for variant and mutation detection in KCNE1 gene for Jervell and Lange-Nielsen syndrome type 2

PreTest Information

Clinical History of Patient who is going for KCNE1 Gene Jervell and Lange-Nielsen syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with KCNE1 Gene Jervell and Lange-Nielsen syndrome type 2 NGS Genetic DNA Test gene KCNE1

Detail Description

KCNE1 Gene Jervell and Lange-Nielsen Syndrome Type 2 NGS Genetic DNA Test Cost INR:20000 Symptoms Diagnosis

Jervell and Lange-Nielsen Syndrome Type 2 is a rare genetic disorder that affects the heart and causes hearing loss. It is caused by mutations in the KCNE1 gene, which codes for a protein that helps regulate the heart’s electrical activity. This disorder is inherited in an autosomal recessive pattern, which means that a person must inherit two copies of the mutated gene, one from each parent, to develop the disorder.

Symptoms of Jervell and Lange-Nielsen Syndrome Type 2

The symptoms of Jervell and Lange-Nielsen Syndrome Type 2 can vary from person to person, but the most common symptoms include:

• Irregular heartbeats
• Fainting spells
• Hearing loss
• Dizziness
• Shortness of breath
• Chest pain
• Palpitations

Diagnosing Jervell and Lange-Nielsen Syndrome Type 2

Jervell and Lange-Nielsen Syndrome Type 2 can be diagnosed through genetic testing. The KCNE1 gene can be sequenced using Next Generation Sequencing (NGS) technology, which allows for the identification of mutations in the gene. If a mutation is identified, a diagnosis can be made. It is important to note that not all mutations in the KCNE1 gene are associated with Jervell and Lange-Nielsen Syndrome Type 2, so it is important to consult a genetic counselor or healthcare provider to determine the appropriate genetic testing strategy.

Cost of Jervell and Lange-Nielsen Syndrome Type 2 NGS Genetic DNA Test

The cost of Jervell and Lange-Nielsen Syndrome Type 2 NGS Genetic DNA Test in India is INR 20,000. This cost may vary depending on the laboratory or healthcare provider performing the test.

Conclusion

Jervell and Lange-Nielsen Syndrome Type 2 is a rare genetic disorder that affects the heart and causes hearing loss. It is caused by mutations in the KCNE1 gene, which can be identified through NGS genetic testing. If you or a loved one is experiencing symptoms of Jervell and Lange-Nielsen Syndrome Type 2, it is important to consult a healthcare provider or genetic counselor to determine the appropriate testing and treatment strategies.

By getting tested, you can get a better understanding of your genetic makeup and take steps to manage your health and prevent complications associated with Jervell and Lange-Nielsen Syndrome Type 2.

At DNA Labs India, we offer NGS Genetic DNA testing for Jervell and Lange-Nielsen Syndrome Type 2. Our state-of-the-art technology and expert genetic counselors ensure that you receive accurate and reliable results. Contact us today to learn more about our genetic testing services.