Biliary atresia
Treatment:
Surgery is usually performed within the first 2 months of life. The surgery connects the liver to the small intestine, bypassing the malformed ducts. A liver transplant may also be recommended to treat certain types of biliary atresia.
Expectations (prognosis):
Early surgical intervention will improve the survival of more than one-third of those affected by the condition. The long-term benefit of liver transplant is not yet known, but is expected to improve survival.
Complications:
Calling your health care provider:
Call for an appointment with your health care provider if your child appears jaundiced, or if other symptoms of this disorder develop.
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