A case report of Lhermitte–Duclos disease revealed by psychiatric disturbances

BACKGROUND: Lhermitte–Duclos disease (LDD) is a rare cerebellar lesion characterized by a hamartomatous lesion in the posterior fossa. Mainly diagnosed by MRI, the clinical presentation is usually made of neurological symptoms. CASE PRESENTATION: We present here a rare case of a woman who developed...

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Detalles Bibliográficos
Autores principales: Otheman, Yassine, Aalouane, Rachid, Aarab, Chadia, Rammouz, Ismail
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5450341/
https://www.ncbi.nlm.nih.gov/pubmed/28572832
http://dx.doi.org/10.1186/s12991-017-0147-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5450341/
https://www.ncbi.nlm.nih.gov/pubmed/28572832
http://dx.doi.org/10.1186/s12991-017-0147-1

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