TY - JOUR
T1 - Dyke–Davidoff–Masson syndrome in a Nigerian
AU - Adebayo, Philip B.
AU - Bakare, Amnat
AU - Bello, Modupe M.
AU - Olaewe, Opeyemi D.
AU - Wahab, Kolawole W.
N1 - Publisher Copyright:
© 2016
PY - 2017
Y1 - 2017
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85007040196&partnerID=8YFLogxK
U2 - 10.1016/j.ebcr.2016.09.003
DO - 10.1016/j.ebcr.2016.09.003
M3 - Article
AN - SCOPUS:85007040196
SN - 2213-3232
VL - 7
SP - 10
EP - 12
JO - Epilepsy and Behavior Case Reports
JF - Epilepsy and Behavior Case Reports
ER -