Najjar Syndrome Crigler Genetic Disorders

Najjar Syndrome Crigler Genetic Disorders

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.

Top: Health: Conditions and Diseases: Genetic Disorders: Crigler-Najjar Syndrome

See Also:

NORD: Crigler Najjar Syndrome Type I - General information and further resources.
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.
Crigler-Najjar Association of America - 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.
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.

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