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Catatonia as presenting clinical feature of subacute sclerosing panencephalitis
Catatonia is not a usual clinical presentation of subacute sclerosing panencephalitis (SSPE), especially in the initial stages of illness. However, there is only one reported case of SSPE presenting as catatonia among children. In this report, however, there were SSPE-specific changes on EEG and the...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4040037/ https://www.ncbi.nlm.nih.gov/pubmed/24891908 http://dx.doi.org/10.4103/1817-1745.131489 |
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author | Dayal, Prabhoo Balhara, Yatan Pal Singh |
author_facet | Dayal, Prabhoo Balhara, Yatan Pal Singh |
author_sort | Dayal, Prabhoo |
collection | PubMed |
description | Catatonia is not a usual clinical presentation of subacute sclerosing panencephalitis (SSPE), especially in the initial stages of illness. However, there is only one reported case of SSPE presenting as catatonia among children. In this report, however, there were SSPE-specific changes on EEG and the catatonia failed to respond to lorazepam. We describe a case of SSPE in a child presenting as catatonia that presented with clinical features of catatonia and did not have typical EEG findings when assessed at first contact. He responded to lorazepam and EEG changes emerged during the course of follow-up. |
format | Online Article Text |
id | pubmed-4040037 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-40400372014-06-02 Catatonia as presenting clinical feature of subacute sclerosing panencephalitis Dayal, Prabhoo Balhara, Yatan Pal Singh J Pediatr Neurosci Case Report Catatonia is not a usual clinical presentation of subacute sclerosing panencephalitis (SSPE), especially in the initial stages of illness. However, there is only one reported case of SSPE presenting as catatonia among children. In this report, however, there were SSPE-specific changes on EEG and the catatonia failed to respond to lorazepam. We describe a case of SSPE in a child presenting as catatonia that presented with clinical features of catatonia and did not have typical EEG findings when assessed at first contact. He responded to lorazepam and EEG changes emerged during the course of follow-up. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4040037/ /pubmed/24891908 http://dx.doi.org/10.4103/1817-1745.131489 Text en Copyright: © Journal of Pediatric Neurosciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Dayal, Prabhoo Balhara, Yatan Pal Singh Catatonia as presenting clinical feature of subacute sclerosing panencephalitis |
title | Catatonia as presenting clinical feature of subacute sclerosing panencephalitis |
title_full | Catatonia as presenting clinical feature of subacute sclerosing panencephalitis |
title_fullStr | Catatonia as presenting clinical feature of subacute sclerosing panencephalitis |
title_full_unstemmed | Catatonia as presenting clinical feature of subacute sclerosing panencephalitis |
title_short | Catatonia as presenting clinical feature of subacute sclerosing panencephalitis |
title_sort | catatonia as presenting clinical feature of subacute sclerosing panencephalitis |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4040037/ https://www.ncbi.nlm.nih.gov/pubmed/24891908 http://dx.doi.org/10.4103/1817-1745.131489 |
work_keys_str_mv | AT dayalprabhoo catatoniaaspresentingclinicalfeatureofsubacutesclerosingpanencephalitis AT balharayatanpalsingh catatoniaaspresentingclinicalfeatureofsubacutesclerosingpanencephalitis |