Encyclopedia Home / C / Crigler-Najjar syndrome

Crigler-Najjar syndrome

  • Alternative Names

    Glucuronyl transferase deficiency (type I Crigler-Najjar); Arias syndrome (type II Crigler-Najjar)


    Treatment

    Light treatment (phototherapy) is needed on a regular basis throughout life. In infants this is done using bilirubin lights (bili or 'blue' lights). Phototherapy becomes less successful after age 4, because thickened skin blocks the light.

    Liver transplantation has been used successfully in some people with type 1 disease.

    Blood transfusions may help control the amount of bilirubin in blood plasma. Calcium compounds are sometimes used to bind with and remove bilirubin in the gut.

    The drug phenobarbitol is sometimes used to treat Arias syndrome (type 2).


    Support Groups


    Expectations (prognosis)

    Milder forms of the disease (type 2) do not cause severe toxicity, liver damage, or changes in thinking during childhood. People affected still have jaundice, but they have fewer symptoms and less organ damage.

    Infants with the severe form of the disease (type 1) may continue to have jaundice into adulthood, and may need daily treatment. If left untreated, this severe form of the disease will lead to death in childhood.

    People with this condition who reach adulthood will develop brain damage due to jaundice (kernicterus), even with regular treatment. The life expectancy for type 1 disease is 30 years.


    Complications

    Possible complications include:

    • A form of brain damage caused by jaundice (kernicterus)
    • Chronic yellow skin/eyes

    Calling your health care provider

    Seek genetic counseling if you are planning to have children and have a family history of Crigler-Najjar.

    Call your health care provider if you or your newborn infant has jaundice that does not go away.