Short Description

NGS genetic DNA test detecets for variant and mutation detection in TJP2 gene for Hypercholanemia

PreTest Information

Clinical History of Patient who is going for TJP2 Gene Hypercholanemia NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Hypercholanemia

Detail Description

DNA Labs India: TJP2 Gene Hypercholanemia NGS Genetic DNA Test

Hypercholanemia is a rare genetic disorder characterized by elevated levels of bile acids in the blood. It is caused by mutations in the TJP2 gene, which encodes a protein that regulates the flow of bile acids into the liver.

The symptoms of hypercholanemia can vary widely, but may include jaundice, itching, fatigue, abdominal pain, and liver damage. Diagnosis is typically made through blood tests and liver function tests.

At DNA Labs India, we offer a TJP2 Gene Hypercholanemia NGS Genetic DNA Test to help diagnose this rare disorder. Our test uses next-generation sequencing (NGS) technology to analyze the entire TJP2 gene, providing a comprehensive analysis of all possible mutations.

The cost of our TJP2 Gene Hypercholanemia NGS Genetic DNA Test is INR 20,000. This includes the cost of the test itself, as well as any necessary counseling and support services.

If you or a loved one are experiencing symptoms of hypercholanemia, it is important to seek medical attention as soon as possible. Our TJP2 Gene Hypercholanemia NGS Genetic DNA Test can help provide a definitive diagnosis, allowing for appropriate treatment and management of this rare disorder.

Don't wait to get the answers you need. Contact DNA Labs India today to learn more about our TJP2 Gene Hypercholanemia NGS Genetic DNA Test.