Asymptomatic Dandy-Walker syndrome in an adult
Hatim Belfquih, Brahim Elmostarchid
The Pan African Medical Journal. ;19:15. doi:10.11604/pamj..19.15.3974

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Asymptomatic Dandy-Walker syndrome in an adult

Hatim Belfquih, Brahim Elmostarchid
Pan Afr Med J. 2014; 19:15. doi:10.11604/pamj.2014.19.15.3974. Published 08 Sep 2014



This 34 years old man presented with moderate and persistent headache occurring 48 hours following Benin head injury. There were no symptoms of increased intracranial pressure. Neurological examination was unremarkable without cerebellar ataxia or psychomotor retardation .the patient was submitted to CT scan and magnetic resonance imaging (MRI) of the brain that revealed agenesis of cerebellar vermis and large posterior fossa cyst communicating with the enlarged fourth ventricle suggestive of Dandy-Walker malformation without hydrocephalus. He was managed conservatively and he is doing well following 2 years ago. The Dandy-Walker syndrome (DWS) is a rare posterior fossa malformation and more rarely observed in adults. This case is unique in that the patient has been entirely asymptomatic with this abnormality since birth. The preserved cortical cytoarchitecture and the rarity of additional neurodevelopmental changes in DWS adults may explain the mild or absence of clinical expression, compared with DWS infants.


Corresponding author:
Hatim Belfquih, Department of Neurosurgery, Mohammed V Military Teaching Hospital, Rabat, Morocco
hatimbelfquih@gmail.com

©Hatim Belfquih et al. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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