Health Conditions and Diseases Nutritional and Metabolic Disorders Inherited
Crigler-Najjar Syndrome
5
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.
More information
More information
Related categories 2
Sites 5
Bi-lingual site with information and links on this disease.
Discusses how this familial form of congenital hyperbilirubinemia, also known as Arias' Syndrome, was named. Includes brief description, synonyms, and associated persons.
Explains this rare disorder, including the two types, diagnosis, experimental treatment, and related links.
Illustrated article details the signs, symptoms, causes, and treatments of type I and type II. Includes risk factors, prognosis, and prevention.
General information and further resources.
Illustrated article details the signs, symptoms, causes, and treatments of type I and type II. Includes risk factors, prognosis, and prevention.
Bi-lingual site with information and links on this disease.
General information and further resources.
Discusses how this familial form of congenital hyperbilirubinemia, also known as Arias' Syndrome, was named. Includes brief description, synonyms, and associated persons.
Explains this rare disorder, including the two types, diagnosis, experimental treatment, and related links.
Last update:
December 7, 2016 at 17:15:02 UTC
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Regional: South America: Brazil: Science and Environment
- Recently edited by shedragon
- Recently edited by shedragon