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Dystonic opisthotonus: A “red flag” for neurodegeneration with brain iron accumulation syndromes?
Back arching was reported in one of the very first patients with neurodegeneration with brain iron accumulation syndrome (NBIAs) published in 1936. However, recent reports have mainly focused on the genetic and imaging aspects of these disorders, and the phenotypic characterization of the dystonia h...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BlackWell Publishing Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4208296/ https://www.ncbi.nlm.nih.gov/pubmed/23736975 http://dx.doi.org/10.1002/mds.25490 |
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author | Stamelou, Maria Lai, Scarlett C Aggarwal, Annu Schneider, Susanne A Houlden, Henry Yeh, Tu-Hsueh Batla, Amit Lu, Chin-Song Bhatt, Mohit Bhatia, Kailash P |
author_facet | Stamelou, Maria Lai, Scarlett C Aggarwal, Annu Schneider, Susanne A Houlden, Henry Yeh, Tu-Hsueh Batla, Amit Lu, Chin-Song Bhatt, Mohit Bhatia, Kailash P |
author_sort | Stamelou, Maria |
collection | PubMed |
description | Back arching was reported in one of the very first patients with neurodegeneration with brain iron accumulation syndrome (NBIAs) published in 1936. However, recent reports have mainly focused on the genetic and imaging aspects of these disorders, and the phenotypic characterization of the dystonia has been lost. In evaluating patients with NBIAs in our centers, we have observed that action-induced dystonic opisthotonus is a common and characteristic feature of NBIAs. Here, we present a case series of patients with NBIAs presenting this feature demonstrated by videos. We suggest that dystonic opisthotonus could be a useful “red flag” for clinicians to suspect NBIAs, and we discuss the differential diagnosis of this feature. This would be particularly useful in identifying patients with NBIAs and no iron accumulation as yet on brain imaging (for example, as in phospholipase A2, group IV (cytosolic, calcium-independent) [PLA2G6]-related disorders), and it has management implications. © 2013 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society. |
format | Online Article Text |
id | pubmed-4208296 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BlackWell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-42082962014-10-24 Dystonic opisthotonus: A “red flag” for neurodegeneration with brain iron accumulation syndromes? Stamelou, Maria Lai, Scarlett C Aggarwal, Annu Schneider, Susanne A Houlden, Henry Yeh, Tu-Hsueh Batla, Amit Lu, Chin-Song Bhatt, Mohit Bhatia, Kailash P Mov Disord Viewpoint Back arching was reported in one of the very first patients with neurodegeneration with brain iron accumulation syndrome (NBIAs) published in 1936. However, recent reports have mainly focused on the genetic and imaging aspects of these disorders, and the phenotypic characterization of the dystonia has been lost. In evaluating patients with NBIAs in our centers, we have observed that action-induced dystonic opisthotonus is a common and characteristic feature of NBIAs. Here, we present a case series of patients with NBIAs presenting this feature demonstrated by videos. We suggest that dystonic opisthotonus could be a useful “red flag” for clinicians to suspect NBIAs, and we discuss the differential diagnosis of this feature. This would be particularly useful in identifying patients with NBIAs and no iron accumulation as yet on brain imaging (for example, as in phospholipase A2, group IV (cytosolic, calcium-independent) [PLA2G6]-related disorders), and it has management implications. © 2013 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society. BlackWell Publishing Ltd 2013-09 2013-06-04 /pmc/articles/PMC4208296/ /pubmed/23736975 http://dx.doi.org/10.1002/mds.25490 Text en © 2013 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Viewpoint Stamelou, Maria Lai, Scarlett C Aggarwal, Annu Schneider, Susanne A Houlden, Henry Yeh, Tu-Hsueh Batla, Amit Lu, Chin-Song Bhatt, Mohit Bhatia, Kailash P Dystonic opisthotonus: A “red flag” for neurodegeneration with brain iron accumulation syndromes? |
title | Dystonic opisthotonus: A “red flag” for neurodegeneration with brain iron accumulation syndromes? |
title_full | Dystonic opisthotonus: A “red flag” for neurodegeneration with brain iron accumulation syndromes? |
title_fullStr | Dystonic opisthotonus: A “red flag” for neurodegeneration with brain iron accumulation syndromes? |
title_full_unstemmed | Dystonic opisthotonus: A “red flag” for neurodegeneration with brain iron accumulation syndromes? |
title_short | Dystonic opisthotonus: A “red flag” for neurodegeneration with brain iron accumulation syndromes? |
title_sort | dystonic opisthotonus: a “red flag” for neurodegeneration with brain iron accumulation syndromes? |
topic | Viewpoint |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4208296/ https://www.ncbi.nlm.nih.gov/pubmed/23736975 http://dx.doi.org/10.1002/mds.25490 |
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