Understanding Cholestasis: Birth Defects and Diagnosis
Learn about birth defects linked to cholestasis, including biliary atresia and Alagille syndrome. Early diagnosis is crucial for newborns.
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Cholestasis is a condition where bile flow from the liver is reduced or blocked. Birth defects associated with it can include biliary atresia, where bile ducts are absent or malformed, and Alagille syndrome, which affects multiple organs. Monitoring liver function and consulting a healthcare provider for proper diagnosis and treatment is crucial if cholestasis is suspected in newborns.
FAQs & Answers
- What is cholestasis? Cholestasis is a liver condition where the flow of bile is reduced or blocked, affecting the digestion of fats and the elimination of toxins.
- What are the birth defects associated with cholestasis? Birth defects associated with cholestasis can include biliary atresia, where bile ducts are absent or malformed, and Alagille syndrome, which impacts various organs.
- How is cholestasis diagnosed in newborns? Diagnosis of cholestasis in newborns typically involves monitoring liver function tests, physical examinations, and potentially imaging studies to assess bile flow.
- What treatment options are available for cholestasis in infants? Treatment options for cholestasis in infants vary based on the underlying cause but may include surgical interventions, medications to improve bile flow, and regular monitoring by a healthcare provider.