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Dyke–Davidoff–Masson syndrome in a Nigerian

Authors :
Philip B. Adebayo
Amnat Bakare
Modupe M. Bello
Opeyemi D. Olaewe
Kolawole W. Wahab
Source :
Epilepsy and Behavior Case Reports, Vol 7, Iss C, Pp 10-12 (2017)
Publication Year :
2017
Publisher :
Elsevier, 2017.

Abstract

Dyke–Davidoff–Masson syndrome (DDMS) is a rare, but important cause of drug-resistant seizures. Dyke–Davidoff–Masson syndrome is a constellation of clinical features that consists of hemiparesis, seizure, facial asymmetry, and intellectual disability with distinct neuroimaging features. A 27-year-old lady presented to us with drug-resistant epilepsy, hemiparesis, and intellectual disability that necessitated her withdrawal from school. Her brain magnetic resonance imaging (MRI) showed cerebral hemiatrophy, calvarial thickening, and hyperpneumatization of the frontal sinuses consistent with DDMS. We discuss the diagnostic and therapeutic implications of DDMS and advocate early referral and evaluation of people with epilepsy in sub-Saharan African settings.

Details

Language :
English
ISSN :
22133232
Volume :
7
Issue :
C
Database :
Directory of Open Access Journals
Journal :
Epilepsy and Behavior Case Reports
Publication Type :
Academic Journal
Accession number :
edsdoj.4cd2f14d75cd4eee91769de7a5a02925
Document Type :
article
Full Text :
https://doi.org/10.1016/j.ebcr.2016.09.003