Search results
Jul 1, 2022 · Gilbert (zheel-BAYR) syndrome is a common, harmless liver condition in which the liver doesn't properly process bilirubin. Bilirubin is produced by the breakdown of red blood cells. The liver is your largest internal organ.
Diagnosis is based on higher levels of unconjugated bilirubin in the blood without either signs of other liver problems or red blood cell breakdown. [2][3] Typically no treatment is needed. [1] Gilbert syndrome is associated with decreased cardiovascular health risks. [4]
Overview. What is Gilbert's syndrome? Gilbert's syndrome is an inherited (genetic) liver disorder that affects the body’s ability to process bilirubin. Bilirubin is yellow liquid waste that occurs naturally as the body breaks down old red blood cells.
Gilbert's syndrome is a genetic condition that runs in families. People with the syndrome have a faulty gene, which causes the liver to have problems removing bilirubin from the blood.
Aug 18, 2020 · Gilbert syndrome is an autosomal recessive disorder of bilirubin metabolism within the liver. [1] [2] Reduced glucuronidation of bilirubin leads to unconjugated hyperbilirubinemia and recurrent episodes of jaundice. [1] Under normal circumstances, approximately 95% of bilirubin is unconjugated.
- 2023/02/06
Jul 13, 2022 · Gilbert's syndrome - also known as constitutional hepatic dysfunction - is a condition where the liver does not process bilirubin very well. It is sometimes called Gilbert's disease although it does not cause 'disease' as such. The liver itself is normal and the condition is harmless.
People also ask
What is Gilbert's syndrome?
How does Gilbert's syndrome affect bilirubin?
How common is Gilbert's syndrome?
What is Gilbert (zheel-Bayr) syndrome?
Sep 18, 2018 · Gilbert’s syndrome is an inherited liver condition in which your liver can’t fully process a compound called bilirubin. Your liver breaks down old red blood cells into compounds,...
