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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.
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Crigler-Najjar Association of America
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Support site for parents and patients with Crigler-Najjar Syndrome Type 1 and Type 2. For physicians and researchers learn about essential treatment to avoid brain damage due to excessive bilirubin concentrations.
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Crigler-Najjar Syndrome
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Bi-lingual site with information and links on this disease.
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Crigler-Najjar Syndrome
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Discusses how this familial form of congenital hyperbilirubinemia, also known as Arias' Syndrome, was named. Includes brief description, synonyms, and associated persons.
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Crigler-Najjar Syndrome
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Details about this inherited disorder include alternative names, causes, risk factors, symptoms, signs and tests, treatment, and prognosis.
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Crigler-Najjar Syndrome
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Explains this rare disorder, including the two types, diagnosis, experimental treatment, and related links.
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MedlinePlus: Crigler-Najjar Syndrome
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Illustrated article details the signs, symptoms, causes, and treatments of type I and type II. Includes risk factors, prognosis, and prevention.
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NORD: Crigler Najjar Syndrome Type I
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General information and further resources.
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