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Case Report and Literature Review: COVID-19 and status epilepticus in Dyke-Davidoff-Masson syndrome
Dyke-Davidoff-Masson syndrome (DMMS) is a non-inherited rare condition with a clinical constellation of hemiparesis/hemiplegia, facial asymmetry, intellectual disability, and epilepsy. The radiological features can be including unilateral cerebral atrophy, calvarial thickening, and hyper pneumatizat...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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F1000 Research Limited
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9214268/ https://www.ncbi.nlm.nih.gov/pubmed/35814634 http://dx.doi.org/10.12688/f1000research.27971.1 |
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author | Ibañez Valdés, Lourdes de Fátima Geroge, Jerry Joseph, Sibi Alshmandi, Mohamed Makaleni, Wendy Foyaca Sibat, Humberto |
author_facet | Ibañez Valdés, Lourdes de Fátima Geroge, Jerry Joseph, Sibi Alshmandi, Mohamed Makaleni, Wendy Foyaca Sibat, Humberto |
author_sort | Ibañez Valdés, Lourdes de Fátima |
collection | PubMed |
description | Dyke-Davidoff-Masson syndrome (DMMS) is a non-inherited rare condition with a clinical constellation of hemiparesis/hemiplegia, facial asymmetry, intellectual disability, and epilepsy. The radiological features can be including unilateral cerebral atrophy, calvarial thickening, and hyper pneumatization of the paranasal sinuses. The condition can either be congenital or acquired. The presentation usually occurs during childhood or early adolescents, but there have been adult cases reported. Here we report a 48-year-old male who was a known poorly controlled epileptic that contracted SARS-CoV-2 with subsequently developed status epilepticus and, when worked up, was shown to have features of DDMS. This case is unique as the patient had hemiatrophy and epilepsy but managed to lead a normal, physically demanding, and high functioning academic career and presented late in life. Perhaps only due to coronavirus disease 2019 (COVID-19) was this diagnosis picked up. This report contains a case presenting atypical DDMS in status epilepticus and COVID -19 plus other complications. From our knowledge, this is the first case presenting these comorbidities reported to the medical literature. |
format | Online Article Text |
id | pubmed-9214268 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | F1000 Research Limited |
record_format | MEDLINE/PubMed |
spelling | pubmed-92142682022-07-08 Case Report and Literature Review: COVID-19 and status epilepticus in Dyke-Davidoff-Masson syndrome Ibañez Valdés, Lourdes de Fátima Geroge, Jerry Joseph, Sibi Alshmandi, Mohamed Makaleni, Wendy Foyaca Sibat, Humberto F1000Res Case Report Dyke-Davidoff-Masson syndrome (DMMS) is a non-inherited rare condition with a clinical constellation of hemiparesis/hemiplegia, facial asymmetry, intellectual disability, and epilepsy. The radiological features can be including unilateral cerebral atrophy, calvarial thickening, and hyper pneumatization of the paranasal sinuses. The condition can either be congenital or acquired. The presentation usually occurs during childhood or early adolescents, but there have been adult cases reported. Here we report a 48-year-old male who was a known poorly controlled epileptic that contracted SARS-CoV-2 with subsequently developed status epilepticus and, when worked up, was shown to have features of DDMS. This case is unique as the patient had hemiatrophy and epilepsy but managed to lead a normal, physically demanding, and high functioning academic career and presented late in life. Perhaps only due to coronavirus disease 2019 (COVID-19) was this diagnosis picked up. This report contains a case presenting atypical DDMS in status epilepticus and COVID -19 plus other complications. From our knowledge, this is the first case presenting these comorbidities reported to the medical literature. F1000 Research Limited 2021-01-08 /pmc/articles/PMC9214268/ /pubmed/35814634 http://dx.doi.org/10.12688/f1000research.27971.1 Text en Copyright: © 2021 Ibañez Valdés LdF et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Ibañez Valdés, Lourdes de Fátima Geroge, Jerry Joseph, Sibi Alshmandi, Mohamed Makaleni, Wendy Foyaca Sibat, Humberto Case Report and Literature Review: COVID-19 and status epilepticus in Dyke-Davidoff-Masson syndrome |
title | Case Report and Literature Review: COVID-19 and status epilepticus in Dyke-Davidoff-Masson syndrome |
title_full | Case Report and Literature Review: COVID-19 and status epilepticus in Dyke-Davidoff-Masson syndrome |
title_fullStr | Case Report and Literature Review: COVID-19 and status epilepticus in Dyke-Davidoff-Masson syndrome |
title_full_unstemmed | Case Report and Literature Review: COVID-19 and status epilepticus in Dyke-Davidoff-Masson syndrome |
title_short | Case Report and Literature Review: COVID-19 and status epilepticus in Dyke-Davidoff-Masson syndrome |
title_sort | case report and literature review: covid-19 and status epilepticus in dyke-davidoff-masson syndrome |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9214268/ https://www.ncbi.nlm.nih.gov/pubmed/35814634 http://dx.doi.org/10.12688/f1000research.27971.1 |
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