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2013 | OriginalPaper | Buchkapitel

21. Infusionstherapie und Ernährung bei angeborenen Stoffwechselstörungen

verfasst von : Prof. Dr. E. Mönch

Erschienen in: Ernährungsmedizin Pädiatrie

Verlag: Springer Berlin Heidelberg

Zusammenfassung

Die Zahl der bekannten angeborenen Stoffwechselstörungen ist in den letzten Jahren auf mehr als 2.000 angestiegen. Bisher behandelbar sind davon aber nur etwa 200. Die hier zur Beschreibung getroffene Auswahl orientiert sich im Wesentlichen an den für das Neugeborenenscreening empfohlenen angeborenen Stoffwechselstörungen (Interdiziplinäre Screeningkommission der Deutschen Gesellschaft für Kinderheilkunde und Jugendmedizin 2002). Statt der sehr seltenen und unterschiedlich zu therapierenden 3 Carnitin-Zyklus-Defekte, des LCHAD- und des VLCAD-Mangels („Differenzialdiagnostik“; ▶ Abschn. 21.5) wird der Ornithintranscarbamylasemangel (OTC-Mangel) exemplarisch für die Störungen in der Harnstoffsynthese und solche Erkrankungen abgehandelt, die mit schwerer Hyperammonämie einhergehen können.
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Metadaten
Titel
Infusionstherapie und Ernährung bei angeborenen Stoffwechselstörungen
verfasst von
Prof. Dr. E. Mönch
Copyright-Jahr
2013
Verlag
Springer Berlin Heidelberg
DOI
https://doi.org/10.1007/978-3-642-29817-2_21

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