Delayed Response to Phenobarbital Treatment of a Crigler-Najjar Type II Patient with Partially Inactivating Missense Mutations in the Bilirubin UDP-Glucuronosyltransferase Gene

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Bibliographische Detailangaben
Veröffentlicht in:	Journal of pediatric gastroenterology and nutrition 1999-02, Vol.28 (2), p.210-213
Hauptverfasser:	Ciotti, Marco, Werlin, Steven L, Owens, Ida S
Format:	Artikel
Sprache:	eng
Schlagworte:	Bilirubin - blood Biological and medical sciences Crigler-Najjar Syndrome - diagnosis Crigler-Najjar Syndrome - drug therapy Crigler-Najjar Syndrome - genetics Errors of metabolism Fluid Therapy Glucuronosyltransferase - genetics Humans Hyperbilirubinemia - genetics Hyperbilirubinemia - therapy Infant, Newborn Male Medical sciences Metabolic diseases Miscellaneous hereditary metabolic disorders Mutation, Missense Phenobarbital - therapeutic use Phototherapy
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