Niemann–Pick disease type C1 presenting with psychosis in an adolescent male
Abstract: Niemann–Pick disease, a neurovisceral lysosomal lipid storage disorder, is a rare disorder that is unknown to many clinicians. The disease, that often has its onset during childhood or adolescence, shows a polymorphic clinical picture, including psychiatric symptoms. Because of its infrequence, Niemann–Pick disease is diagnosed with an average delay of 6 years. This report presents a case of an adolescent male whose symptoms had led to various hospitalisations and psychiatric diagnoses. When he presented with psychotic symptoms in our department, thorough diagnosis revealed Niemann–Pick disease type C1 as the underlying disease
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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Postprint
begutachtet (peer reviewed)
In: European Child & Adolescent Psychiatry ; 18 (2009) 9 ; 583-585
- Event
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Veröffentlichung
- (where)
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Mannheim
- (when)
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2009
- Creator
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Sandu, Sabine
Jackowski-Dohrmann, Sabine
Ladner, Axel
Haberhausen, Michael
Bachmann, Christian
- DOI
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10.1007/s00787-009-0010-2
- URN
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urn:nbn:de:0168-ssoar-202676
- Rights
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Open Access unbekannt; Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
25.03.2025, 1:55 PM CET
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Sandu, Sabine
- Jackowski-Dohrmann, Sabine
- Ladner, Axel
- Haberhausen, Michael
- Bachmann, Christian
Time of origin
- 2009
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