Dyke-Davidoff-Masson syndrome: A case report with a literature review()

Dyke-Davidoff-Masson syndrome (DDMS) is an uncommon neurological disease defined as cerebral hemiatrophy with a contralateral motor deficit, facial asymmetry, and seizures. Classic imaging findings are cerebral hypoplasia, ventriculomegaly, paranasal sinus hyper-pneumatization, and compensatory osse...

Descripción completa

Detalles Bibliográficos
Autores principales: Hamid, Mohamed, Cherradi, Soukaina, Satte, Amal, Bourazza, Ahmed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9157201/
https://www.ncbi.nlm.nih.gov/pubmed/35663814
http://dx.doi.org/10.1016/j.radcr.2022.04.047
_version_ 1784718589580804096
author Hamid, Mohamed
Cherradi, Soukaina
Satte, Amal
Bourazza, Ahmed
author_facet Hamid, Mohamed
Cherradi, Soukaina
Satte, Amal
Bourazza, Ahmed
author_sort Hamid, Mohamed
collection PubMed
description Dyke-Davidoff-Masson syndrome (DDMS) is an uncommon neurological disease defined as cerebral hemiatrophy with a contralateral motor deficit, facial asymmetry, and seizures. Classic imaging findings are cerebral hypoplasia, ventriculomegaly, paranasal sinus hyper-pneumatization, and compensatory osseous enlargement. The diagnosis of DDMS is based on the correlation between clinical and neuroimaging features. The management of DDMS is based on anticonvulsant medication with physiotherapy. We describe an unusual case of DDMS presented with frequent and persistent seizures.
format Online
Article
Text
id pubmed-9157201
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-91572012022-06-02 Dyke-Davidoff-Masson syndrome: A case report with a literature review() Hamid, Mohamed Cherradi, Soukaina Satte, Amal Bourazza, Ahmed Radiol Case Rep Case Report Dyke-Davidoff-Masson syndrome (DDMS) is an uncommon neurological disease defined as cerebral hemiatrophy with a contralateral motor deficit, facial asymmetry, and seizures. Classic imaging findings are cerebral hypoplasia, ventriculomegaly, paranasal sinus hyper-pneumatization, and compensatory osseous enlargement. The diagnosis of DDMS is based on the correlation between clinical and neuroimaging features. The management of DDMS is based on anticonvulsant medication with physiotherapy. We describe an unusual case of DDMS presented with frequent and persistent seizures. Elsevier 2022-05-28 /pmc/articles/PMC9157201/ /pubmed/35663814 http://dx.doi.org/10.1016/j.radcr.2022.04.047 Text en © 2022 The Authors. Published by Elsevier Inc. on behalf of University of Washington. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Hamid, Mohamed
Cherradi, Soukaina
Satte, Amal
Bourazza, Ahmed
Dyke-Davidoff-Masson syndrome: A case report with a literature review()
title Dyke-Davidoff-Masson syndrome: A case report with a literature review()
title_full Dyke-Davidoff-Masson syndrome: A case report with a literature review()
title_fullStr Dyke-Davidoff-Masson syndrome: A case report with a literature review()
title_full_unstemmed Dyke-Davidoff-Masson syndrome: A case report with a literature review()
title_short Dyke-Davidoff-Masson syndrome: A case report with a literature review()
title_sort dyke-davidoff-masson syndrome: a case report with a literature review()
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9157201/
https://www.ncbi.nlm.nih.gov/pubmed/35663814
http://dx.doi.org/10.1016/j.radcr.2022.04.047
work_keys_str_mv AT hamidmohamed dykedavidoffmassonsyndromeacasereportwithaliteraturereview
AT cherradisoukaina dykedavidoffmassonsyndromeacasereportwithaliteraturereview
AT satteamal dykedavidoffmassonsyndromeacasereportwithaliteraturereview
AT bourazzaahmed dykedavidoffmassonsyndromeacasereportwithaliteraturereview

Ejemplares similares