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Prise en charge médicale et diététique des maladies héréditaires du métabolisme pp 327–331Cite as

Défaut de glycosylation des glycoprotéines (CDG)

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Résumé

Les anomalies congénitales de glycosylation ou CDG (Congenital Disorders of Glycosylation) forment une classe d’erreurs innées du métabolisme, affectant la synthèse des glycannes des glycoprotéines [1, 2]. La glycosylation fait partie des modifications post-traductionnelles et concerne différents types de structures glycannes, la plus connue étant la N-glycosylation.

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Références

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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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De Lonlay, P., Dubois, S., Valayannopoulos, V., Depondt, E., Ottolenghi, C., Rabier, D. (2013). Défaut de glycosylation des glycoprotéines (CDG). In: Prise en charge médicale et diététique des maladies héréditaires du métabolisme. Springer, Paris. https://doi.org/10.1007/978-2-8178-0046-2_23

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  • DOI: https://doi.org/10.1007/978-2-8178-0046-2_23

  • Publisher Name: Springer, Paris

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