A case report of Lhermitte–Duclos disease revealed by psychiatric disturbances
Abstract 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 dev...
Main Authors: | , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2017-05-01
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Series: | Annals of General Psychiatry |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s12991-017-0147-1 |