Gilbert's Syndrome - Causes, Symptoms and Treatment Methods

Gilbert's syndrome is a harmless condition but ofteninherited abnormality that causes reduced production
causes anxiety before the condition is diagnosed. It isof an enzyme involved in processing bilirubin. It is
arguably the most common medical syndromeoften first diagnosed in the late teens or early
identified.Gilbert's Syndrome is detected by finding atwenties.
slightly raised bilirubin level in the blood with no otherCauses of Gilbert's syndrome
abnormalities of liver function and no signs of liverThe common causes and risk factor's of Gilbert's
disease. It is the most common hereditary cause ofsyndrome include the following:
increased bilirubin, and is found in up to 5% of theMutation in the UDP-glucuronosyltransferase gene.
population. Unconjugated hyperbilirubinemia in GilbertFasting: This produces an increase in the plasma
syndrome has long been recognized as due tounconjugated bilirubin level.
underactivity of the conjugating enzyme systemStress, such as trauma and overexertion.
bilirubin-uridine diphosphate glucuronyl transferase. TheMenstrual periods.
main symptom is otherwise harmless jaundice whichIntercurrent illness, such as a viral infection.
does not require treatment, caused by elevatedSymptoms of Gilbert's syndrome
levels of unconjugated bilirubin in the bloodstream.Some sign and symptoms related to Gilbert's
Also known as constitutional hepatic dysfunction,syndrome are as follows:
unconjugated benign bilirubinemia and familialGilbert's Syndrome is generally harmless and does not
nonhemolytic jaundice, Gilbert's syndrome typicallyproduce any symptoms, although some sufferers
doesn't require treatment or pose seriouscomplain of excessive fatigue.
complications. Bilirubin levels tend particularly to beMild jaundice (yellowing of skin and whites of eyes).
increased in Gilbert syndrome with starvation orLoss of appetite.
dehydration.Pain in the abdomen (uncommon).
Gilbert's syndrome is most often recognised in theWeakness.
second or third decade of life and is rarely diagnosedTreatment of Gilbert's syndrome
before puberty. Men are often affected more thanHere is list of the methods for treating Gilbert's
women. It can also frequently coexist with thesyndrome:
conditions associated with unconjugatedGilbert's syndrome seems to be a lifelong disorder,
hyperbilirubinemia, such as thalassemia andbut it usually doesn't need medical treatment.
glucose-6-phosphate deficiency. Gilbert's is oftenMedication that helps the enzyme work better may
diagnosed in the late teens and early twenties. Thebe used to treat the jaundice if it becomes a
condition is inherited and is relatively common beingproblem.
estimated to affect about 1 person in 20. The sourcePhenobarbitone in small doses can sometimes help
of this hyperbilirubinemia is reduced activity of theclear the jaundice.
enzyme (glucuronyl transferase) which conjugatesPeople with Gilbert's syndrome don't typically need
bilirubin and some other lipophilic molecules. In peoplelong-term monitoring of their condition or repeat
with Gilbert's syndrome, the bilirubin level often goesblood tests.
up and down. At times, it may be within the normalIf you're distressed by jaundice, the barbiturate
range. People with Gilbert's syndrome have anmedication phenobarbital may reduce bilirubin levels.