An inherited disorder of bilirubin metabolism in which bilirubin cannot be changed into its water-soluble form, bilirubin glucuronide. This is caused by an enzyme imbalance in the liver.

Related categories 2

Crigler-Najjar Syndrome
Explains this rare disorder, including the two types, diagnosis, experimental treatment, and related links.
Crigler-Najjar Syndrome
Discusses how this familial form of congenital hyperbilirubinemia, also known as Arias' Syndrome, was named. Includes brief description, synonyms, and associated persons.
Crigler-Najjar Syndrome
Bi-lingual site with information and links on this disease.
Crigler-Najjar Syndrome
Factsheet about this inherited disorder include alternative names, causes, risk factors, symptoms, signs and tests, treatment and prognosis.
MedlinePlus: Crigler-Najjar Syndrome
Illustrated article details the signs, symptoms, causes, and treatments of type I and type II. Includes risk factors, prognosis, and prevention.
NORD: Crigler Najjar Syndrome Type I
General information and further resources.
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Last update:
October 18, 2016 at 3:02:28 UTC
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