作者: H. L. Rayner , B. A. Schacter , L. G. Israels
DOI: 10.1007/978-3-642-66763-3_10
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摘要: Type I: A hereditary disorder of bilirubin metabolism in which glucuronyl transferase activity is lacking abd the bile free glucuronide. Severe unconjugated hyperbilirubinemia usually leads to kernicterus infancy.