Alagille syndrome is a genetic disorder that affects primarily the liver and the heart. Problems associated with the disorder generally become evident in infancy or early childhood. The disorder is inherited in an autosomal dominant pattern, and the estimated prevalence of Alagille syndrome is 1 in every 100,000 live births. It is named after the French pediatrician Daniel Alagille, who first described the condition in 1969.
The severity of the disorder can vary within the same family, with symptoms ...
ウィキペディアでもっと読む