![]() ![]() People with the syndrome have a faulty gene which causes the liver to have problems removing bilirubin from the blood. Gilbert’s syndrome is a genetic disorder that's hereditary (it runs in families). If you've been diagnosed with Gilbert’s syndrome (see below), you don't usually need to seek medical advice during an episode of jaundice, unless you have additional or unusual symptoms. If you can't get in touch with your GP, contact GP out of hours service for advice. It's important to seek immediate medical advice from your GP if you have jaundice. ![]() But jaundice can be associated with more serious liver problems, such as cirrhosis or hepatitis C. ![]() The jaundice of Gilbert's syndrome is usually mild. You should see your GP if you experience an episode of jaundice for the first time. You may not realise you have the syndrome until tests for an unrelated problem are carried out. These problems aren't necessarily thought to be directly related to increased bilirubin levels and could be related to a condition other than Gilbert’s syndrome.Īround one in three people with Gilbert’s syndrome don't experience any symptoms at all. problems concentrating and thinking clearly (brain fog).irritable bowel syndrome (IBS) – a common digestive disorder that causes stomach cramps, bloating, diarrhoea and constipation.Some people also report other problems during episodes of jaundice, including: Most people with Gilbert's syndrome experience occasional and short-lived episodes of jaundice (yellowing of the skin and whites of the eyes) due to the build-up of bilirubin in the blood.Īs Gilbert's syndrome usually only causes a slight increase in bilirubin levels, the yellowing of jaundice is often mild. It forms when old red blood cells are broken down. Bilirubin is a yellow substance found naturally in the blood. Gilbert's syndrome causes slightly higher than normal levels of a substance called bilirubin to build up in the blood. ![]()
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