Gilbert's syndrome
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Gilbert's syndrome
Gastro
Gastro
Esophageal motility
Gastric motility
Carbohydrates and sugars
Fats and lipids
Proteins
Pancreatic secretion
Bile secretion and enterohepatic circulation
Gastroesophageal reflux disease (GERD)
Esophageal cancer
Eosinophilic esophagitis (NORD)
Peptic ulcer
Gastroschisis
Omphalocele
Intestinal atresia
Hirschsprung disease
Intussusception
Celiac disease
Lactose intolerance
Ulcerative colitis
Crohn disease
Bowel obstruction
Volvulus
Gallstone ileus
Small bowel ischemia and infarction
Ischemic colitis
Familial adenomatous polyposis
Irritable bowel syndrome
Crigler-Najjar syndrome
Gilbert's syndrome
Rotor syndrome
Dubin-Johnson syndrome
Jaundice
Portal hypertension
Hemochromatosis
Cholestatic liver disease
Autoimmune hepatitis
Primary sclerosing cholangitis
Cirrhosis
Hepatic encephalopathy
Wilson disease
Non-alcoholic fatty liver disease
Alcohol-associated liver disease
Viral hepatitis
Hepatocellular carcinoma
Gallstones
Acute cholecystitis
Chronic cholecystitis
Biliary colic
Ascending cholangitis
Acute pancreatitis
Chronic pancreatitis
Pancreatic cancer
Jaundice: Pathology review
Viral hepatitis: Pathology review
Cirrhosis: Pathology review
Laxatives and cathartics
Acid reducing medications
Antidiarrheals
Key Takeaways
Gilbert's syndrome is a genetic disorder that affects how the liver conjugates bilirubin. People with Gilbert's syndrome have mild jaundice, which unusually appears under stressful conditions. The disorder is typically passed down through families in an autosomal recessive pattern, meaning both parents will pass on the gene for a child to be affected.