Gilbert-Lerboulet Syndrome

Gilbert (Lagerble) syndrome is a rare hereditary disease associated with impaired liver function. It is characterized by periodic attacks of jaundice caused by periodic blockage of the bile duct. This condition can be caused by both genetic and physical factors such as liver injury

Gilbert-Lerbullier Syndrome (GLS) is a rare hereditary disease that occurs due to a genetic mutation that leads to disruption of liver and pancreatic enzymes. It manifests itself in patients with impaired normal liver function, which is why GHL is also called “hepatic hypoplasia.”

Genetic testing for gallstone disease may be useful for those people who are at high risk of developing the disease. It will help identify the presence of this mutation in the genome and take appropriate measures, for example, limiting alcohol consumption, avoiding strong medications