Crigler Najjar Syndrome Type I

Vital
It is feasible that the major title of the record Crigler Najjar Syndrome is not the name you anticipated. Uridine Diphosphate Glucuronosyltransferase, Severe Def.
Crigler-Najjar disorder is an unusual hereditary condition defined by raised degrees of bilirubin in the blood (hyperbilirubinemia). The characteristic searching for of Crigler-Najjar disorder is consistent yellowing of the skin, mucous membrane layers and also whites of the eyes (jaundice). There are 2 types of this condition: Crigler-Najjar disorder kind I, defined by a virtually total absence of enzyme task and also serious signs and symptoms; as well as Crigler-Najjar disorder kind II, defined by partial enzyme task as well as milder signs.