Refractory Seizure in Childhood: Dyke-Davidoff-Masson Syndrome Revisited
Dyke-Davidoff-Masson syndrome (DDMS) is a rare disorder characterized by recurrent seizures, facial asymmetry, contralateral hemiplegia, radiologic features of cerebral hemiatrophy, and ipsilateral compensatory hypertrophy of the skull bone and sinuses. We describe three cases of children with DDMS,...
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doaj-7da3ee6021524132ac2c5aaf761787792020-11-24T22:39:17ZengOman Medical Specialty BoardOman Medical Journal1999-768X2070-52042016-07-0131430430810.5001/omj.2016.58Refractory Seizure in Childhood: Dyke-Davidoff-Masson Syndrome RevisitedAbhijit Dutta0Sagar Bose1Kaushik Sen2Narayan Pandit3Samarth Sharma4Department of Pediatric Medicine, North Bengal Medical College and Hospital, Darjeeling, IndiaDepartment of Neurology, K.P.C. Medical College, Kolkata, IndiaDepartment of General Medicine, North Bengal Medical College and Hospital, Darjeeling, IndiaDepartment of Radiology, North Bengal Medical College and Hospital, Darjeeling, IndiaDepartment of General Medicine, North Bengal Medical College and Hospital, Darjeeling, IndiaDyke-Davidoff-Masson syndrome (DDMS) is a rare disorder characterized by recurrent seizures, facial asymmetry, contralateral hemiplegia, radiologic features of cerebral hemiatrophy, and ipsilateral compensatory hypertrophy of the skull bone and sinuses. We describe three cases of children with DDMS, who initially presented with refractory seizure to the pediatric department of North Bengal Medical College and Hospital, India. In each case, the clinical features noted along with computed tomography or magnetic resonance imaging helped confirm the diagnosis of DDMS. DDMS should be considered as a differential diagnosis of refractory seizures in children. We seek to emphasize the importance of thorough clinical and neuroimaging workup of seizure disorder in children for the proper management of the condition.http://omjournal.org/articleDetails.aspx?coType=1&aId=1794Dyke-Davidoff-Masson Syndrome |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Abhijit Dutta Sagar Bose Kaushik Sen Narayan Pandit Samarth Sharma |
spellingShingle |
Abhijit Dutta Sagar Bose Kaushik Sen Narayan Pandit Samarth Sharma Refractory Seizure in Childhood: Dyke-Davidoff-Masson Syndrome Revisited Oman Medical Journal Dyke-Davidoff-Masson Syndrome |
author_facet |
Abhijit Dutta Sagar Bose Kaushik Sen Narayan Pandit Samarth Sharma |
author_sort |
Abhijit Dutta |
title |
Refractory Seizure in Childhood: Dyke-Davidoff-Masson Syndrome Revisited |
title_short |
Refractory Seizure in Childhood: Dyke-Davidoff-Masson Syndrome Revisited |
title_full |
Refractory Seizure in Childhood: Dyke-Davidoff-Masson Syndrome Revisited |
title_fullStr |
Refractory Seizure in Childhood: Dyke-Davidoff-Masson Syndrome Revisited |
title_full_unstemmed |
Refractory Seizure in Childhood: Dyke-Davidoff-Masson Syndrome Revisited |
title_sort |
refractory seizure in childhood: dyke-davidoff-masson syndrome revisited |
publisher |
Oman Medical Specialty Board |
series |
Oman Medical Journal |
issn |
1999-768X 2070-5204 |
publishDate |
2016-07-01 |
description |
Dyke-Davidoff-Masson syndrome (DDMS) is a rare disorder characterized by recurrent seizures, facial asymmetry, contralateral hemiplegia, radiologic features of cerebral hemiatrophy, and ipsilateral compensatory hypertrophy of the skull bone and sinuses. We describe three cases of children with DDMS, who initially presented with refractory seizure to the pediatric department of North Bengal Medical College and Hospital, India. In each case, the clinical features noted along with computed tomography or magnetic resonance imaging helped confirm the diagnosis of DDMS. DDMS should be considered as a differential diagnosis of refractory seizures in children. We seek to emphasize the importance of thorough clinical and neuroimaging workup of seizure disorder in children for the proper management of the condition. |
topic |
Dyke-Davidoff-Masson Syndrome |
url |
http://omjournal.org/articleDetails.aspx?coType=1&aId=1794 |
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