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Prise en charge médicale et diététique des maladies héréditaires du métabolisme pp 401–404Cite as

Cholestase

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Résumé

Le diagnostic de cholestase (défaut de synthèse ou d’excrétion de la bile) peut être:

  • clinique (ictère avec selles décolorées et/ou urines foncées, prurit);

  • ou biologique: augmentation de la bilirubine conjuguée, augmentation des gamma GT et/ou des sels biliaires sériques [1].

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Références

  1. Haber B, Ferreira CT, Aw M, et al. (2008) Cholestasis: current issues and plan for the future. J Pediatr Gastroenterol Nutr 47: 220–4

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  2. Maisels MJ, Bhutani VK, Bogen D, et al. (2009) Hyperbilirubinemia in the newborn infant > or =35 weeks’ gestation: an update with clarifications. Pediatrics 124: 1193–8

    Article  PubMed  Google Scholar 

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Authors and Affiliations

  1. Centre de Référence des maladies héréditaires du métabolisme, Hôpital Necker-Enfants malades, 149, rue de Sèvres, 75743, Paris Cedex 15, France

    Pascale De Lonlay, Sandrine Dubois & Vassili Valayannopoulos

  2. Service de maladies héréditaires du métabolisme, Hôpital Necker-Enfants malades, 149, rue de Sèvres, 75743, Paris Cedex 15, France

    Eliane Depondt

  3. Service de biochimie métabolique Centre de Référence des maladies héréditaires du métabolisme, Hôpital Necker-Enfants malades, 149, rue de Sèvres, 75743, Paris Cedex 15, France

    Chris Ottolenghi & Daniel Rabier

Authors
  1. Pascale De Lonlay
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  2. Sandrine Dubois
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  3. Vassili Valayannopoulos
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  4. Eliane Depondt
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  5. Chris Ottolenghi
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  6. Daniel Rabier
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© 2013 Springer-Verlag France

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De Lonlay, P., Dubois, S., Valayannopoulos, V., Depondt, E., Ottolenghi, C., Rabier, D. (2013). Cholestase. In: Prise en charge médicale et diététique des maladies héréditaires du métabolisme. Springer, Paris. https://doi.org/10.1007/978-2-8178-0046-2_32

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  • DOI: https://doi.org/10.1007/978-2-8178-0046-2_32

  • Publisher Name: Springer, Paris

  • Print ISBN: 978-2-8178-0045-5

  • Online ISBN: 978-2-8178-0046-2

  • eBook Packages: MedicineMedicine (R0)

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