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- W3200764213 abstract "Crigler-Najjar syndrome is a rare autosomal recessive inherited non-hemolytic unconjugated hyperbilirubinemia caused by UDP-glucuronosyltransferase deficiency. There are two forms of this disorder. Type 1 disease is associated with severe jaundice and neurologic impairment due to bilirubin encephalopathy that can result in permanent neurologic sequelae. Type 2 disease is associated with a lower serum bilirubin concentration and affected patients survive into adulthood without neurologic impairment. Currently, liver transplantation is the only available therapeutic method for these patients. Developing new curative approaches is a clinical need." @default.
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- W3200764213 date "2021-08-01" @default.
- W3200764213 modified "2023-09-29" @default.
- W3200764213 title "Management of Crigler-Najjar syndrome." @default.
- W3200764213 doi "https://doi.org/10.15386/mpr-2234" @default.
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