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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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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.
Discusses how this familial form of congenital hyperbilirubinemia, also known as Arias' Syndrome, was named. Includes brief description, synonyms, and associated persons.
General information and further resources.
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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