Successful Plasmapheresis for Acute and Severe Unconjugated Hyperbilirubinemia in a Child with Crigler Najjar Type I Syndrome

Crigler–Najjar syndrome type I (CN-I, MIM #218800) is a rare and severe autosomal disorder. It is caused by deficiency of the liver enzyme responsible for bilirubin elimination, the uridine diphosphate glucuronosyltransferase 1A1 (UGT1A1; EC 2.4.1.17). Biologically, the disease manifests itself with...

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Détails bibliographiques
Auteurs principaux: Sellier, Anne Laure, Labrune, Philippe, Kwon, Theresa, Boudjemline, Alix Mollet, Deschènes, Georges, Gajdos, Vincent
Format: Artigo
Langue:Inglês
Publié: Springer Berlin Heidelberg 2011
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Article
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3509837/
https://ncbi.nlm.nih.gov/pubmed/23430851
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/8904_2011_40
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