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Biliary atresia
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Biliary atresia

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Biliary atresia is a blockage in the tubes (ducts) that carry a liquid called bile from the liver to the gallbladder.

Biliary atresia occurs when the bile ducts inside or outside the liver do not develop normally. The reason why this happens is unknown.

The bile ducts help remove waste from the liver and carry salts that help the small intestine break down (digest) fat.

In babies with biliary atresia, bile flow from the liver to the gallbladder is blocked. This can lead to liver damage and cirrhosis of the liver, which can be deadly.

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  • Causes

    Biliary atresia occurs when the bile ducts inside or outside the liver do not develop normally. The reason why this happens is unknown.

    The bile ducts help remove waste from the liver and carry salts that help the small intestine break down (digest) fat.

    In babies with biliary atresia, bile flow from the liver to the gallbladder is blocked. This can lead to liver damage and cirrhosis of the liver, which can be deadly.

  • Symptoms

    Newborns with this condition may appear normal at birth. However, jaundice (a yellow color to the skin and mucus membranes) develops by the second or third week of life. The infant may gain weight normally for the first month. After that point, the baby will lose weight and become irritable, and will have worsening jaundice.

    Other symptoms may include:

    • Dark urine
    • Enlarged spleen
    • Floating stools
    • Foul-smelling stools
    • Pale or clay-colored stools
    • Slow growth
    • Slow or no weight gain
  • Exams and Tests

    The health care provider will perform a physical exam, which includes feeling the patient's belly area. The doctor may feel an enlarged liver.

    Tests to diagnose biliary atresia include:

    • Abdominal x-ray
    • Abdominal ultrasound
    • Blood tests to check total and direct bilirubin levels
    • Hepatobiliary iminodiacetic acid (HIDA) scan, also called cholescintigraphy, to help determine whether the bile ducts and gallbladder are working properly
    • Liver biopsy to determine the severity of cirrhosis or to rule out other causes of jaundice
    • X-ray of the bile ducts (cholangiogram)
  • Treatment

    An operation called the Kasai procedure is done to connect the liver to the small intestine. The abnormal ducts are bypassed. It is most successful if done before the baby is 8 weeks old. However, a liver transplant may still be needed.

  • Outlook (Prognosis)

    Early surgery will improve the survival of more than a third of babies with this condition. The long-term benefit of a liver transplant is not yet known, but it is expected to improve survival.

  • Possible Complications


    • Infection
    • Irreversible cirrhosis
    • Liver failure
    • Surgical complications, including failure of the Kasai procedure
  • When to Contact a Medical Professional

    Call your health care provider if your child appears jaundiced, or if other symptoms of biliary atresia develop.

Related Information

  BileBiliary systemCirrhosisWeight loss - unin...   Newborn jaundice -...Newborn jaundice -...   Cirrhosis

References

A-Kader HH, Balistreri WF. Neonatal cholestasis. In: Kliegman RM, Behrman RE, Jenson HB, Stanton BF, eds. Nelson Textbook of Pediatrics. 19th ed. Philadelphia, PA: Saunders Elsevier; 2011:chap 348.1.

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Review Date: 5/14/2014  

Reviewed By: Neil K. Kaneshiro, MD, MHA, Clinical Assistant Professor of Pediatrics, University of Washington School of Medicine, Seattle, WA. Also reviewed by David Zieve, MD, MHA, Isla Ogilvie, PhD, and the A.D.A.M. Editorial team.

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