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Erschienen in: medizinische genetik 1/2016

01.03.2016 | Intelligenzminderung | Übersichten

Neuropädiatrische Differenzialdiagnostik der Mikrozephalie im Kindesalter

verfasst von: Maja von der Hagen, Julia B. Hennermann, Horst von Bernuth, Rainer John, Birgit Spors, PD Dr. Angela M. Kaindl

Erschienen in: medizinische genetik | Ausgabe 1/2016

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Zusammenfassung

Eine Mikrozephalie betrifft 2–3 % der Bevölkerung und geht oftmals mit einer Intelligenzminderung einher. Die zugrunde liegende Reduktion des Gehirnvolumens kann sowohl durch exogene Faktoren als auch durch genetische Ursachen bedingt sein. Problematisch sind sowohl die uneinheitliche Klassifikation als auch die große Heterogenität der hinter dem klinischen Zeichen Mikrozephalie stehenden Erkrankungen. Im vorliegenden Artikel stellen wir unseren Vorschlag für die diagnostische Herangehensweise an ein Kind mit Mikrozephalie aus neuropädiatrischer Sicht vor.
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Metadaten
Titel
Neuropädiatrische Differenzialdiagnostik der Mikrozephalie im Kindesalter
verfasst von
Maja von der Hagen
Julia B. Hennermann
Horst von Bernuth
Rainer John
Birgit Spors
PD Dr. Angela M. Kaindl
Publikationsdatum
01.03.2016
Verlag
Springer Berlin Heidelberg
Erschienen in
medizinische genetik / Ausgabe 1/2016
Print ISSN: 0936-5931
Elektronische ISSN: 1863-5490
DOI
https://doi.org/10.1007/s11825-016-0081-7

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