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Niemann–Pick disease type C1 presenting with psychosis in an adolescent male
[Zeitschriftenartikel]
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, Niem... mehr
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.... weniger
Klassifikation
psychische Störungen, Behandlung und Prävention
Freie Schlagwörter
Adolescence; Niemann–Pick disease; Organic psychosis; Sphingomyelin lipidosis
Sprache Dokument
Englisch
Publikationsjahr
2009
Seitenangabe
S. 583-585
Zeitschriftentitel
European Child & Adolescent Psychiatry, 18 (2009) 9
DOI
https://doi.org/10.1007/s00787-009-0010-2
Status
Postprint; begutachtet (peer reviewed)
Lizenz
PEER Licence Agreement (applicable only to documents from PEER project)