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Diagnosis and Management of Opsoclonus-Myoclonus-Ataxia Syndrome in Children: An International Perspective
BACKGROUND AND OBJECTIVES: Opsoclonus-myoclonus-ataxia syndrome (OMAS) is a rare disorder of the nervous system that classically presents with a combination of characteristic eye movement disorder and myoclonus, in addition to ataxia, irritability, and sleep disturbance. There is good evidence that...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8906188/ https://www.ncbi.nlm.nih.gov/pubmed/35260471 http://dx.doi.org/10.1212/NXI.0000000000001153 |
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author | Rossor, Thomas Yeh, E. Ann Khakoo, Yasmin Angelini, Paola Hemingway, Cheryl Irani, Sarosh R. Schleiermacher, Gudrun Santosh, Paramala Lotze, Tim Dale, Russell C. Deiva, Kumaran Hero, Barbara Klein, Andrea de Alarcon, Pedro Gorman, Mark P. Mitchell, Wendy G. Lim, Ming |
author_facet | Rossor, Thomas Yeh, E. Ann Khakoo, Yasmin Angelini, Paola Hemingway, Cheryl Irani, Sarosh R. Schleiermacher, Gudrun Santosh, Paramala Lotze, Tim Dale, Russell C. Deiva, Kumaran Hero, Barbara Klein, Andrea de Alarcon, Pedro Gorman, Mark P. Mitchell, Wendy G. Lim, Ming |
author_sort | Rossor, Thomas |
collection | PubMed |
description | BACKGROUND AND OBJECTIVES: Opsoclonus-myoclonus-ataxia syndrome (OMAS) is a rare disorder of the nervous system that classically presents with a combination of characteristic eye movement disorder and myoclonus, in addition to ataxia, irritability, and sleep disturbance. There is good evidence that OMAS is an immune-mediated condition that may be paraneoplastic in the context of neuroblastoma. This syndrome may be associated with long-term cognitive impairment, yet it remains unclear how this is influenced by disease course and treatment. Treatment is largely predicated on immune suppression, but there is limited evidence to indicate an optimal regimen. METHODS: Following an international multiprofessional workshop in 2004, a body of clinicians and scientists comprising the International OMS Study group continued to meet biennially in a joint professionals and family workshop focusing on pediatric OMAS. Seventeen years after publication of the first report, a writing group was convened to provide a clinical update on the definitions and clinical presentation of OMAS, biomarkers and the role of investigations in a child presenting with OMAS, treatment and management strategies including identification and support of long-term sequelae. RESULTS: The clinical criteria for diagnosis were reviewed, with a proposed approach to laboratory and radiologic investigation of a child presenting with possible OMAS. The evidence for an upfront vs escalating treatment regimen was reviewed, and a treatment algorithm proposed to recognize both these approaches. Importantly, recommendations on monitoring of immunotherapy response and longer-term follow-up based on an expert consensus are provided. DISCUSSION: OMAS is a rare neurologic condition that can be associated with poor cognitive outcomes. This report proposes an approach to investigation and treatment of children presenting with OMAS, based on expert international opinion recognizing the limited data available. |
format | Online Article Text |
id | pubmed-8906188 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-89061882022-03-09 Diagnosis and Management of Opsoclonus-Myoclonus-Ataxia Syndrome in Children: An International Perspective Rossor, Thomas Yeh, E. Ann Khakoo, Yasmin Angelini, Paola Hemingway, Cheryl Irani, Sarosh R. Schleiermacher, Gudrun Santosh, Paramala Lotze, Tim Dale, Russell C. Deiva, Kumaran Hero, Barbara Klein, Andrea de Alarcon, Pedro Gorman, Mark P. Mitchell, Wendy G. Lim, Ming Neurol Neuroimmunol Neuroinflamm Views & Reviews BACKGROUND AND OBJECTIVES: Opsoclonus-myoclonus-ataxia syndrome (OMAS) is a rare disorder of the nervous system that classically presents with a combination of characteristic eye movement disorder and myoclonus, in addition to ataxia, irritability, and sleep disturbance. There is good evidence that OMAS is an immune-mediated condition that may be paraneoplastic in the context of neuroblastoma. This syndrome may be associated with long-term cognitive impairment, yet it remains unclear how this is influenced by disease course and treatment. Treatment is largely predicated on immune suppression, but there is limited evidence to indicate an optimal regimen. METHODS: Following an international multiprofessional workshop in 2004, a body of clinicians and scientists comprising the International OMS Study group continued to meet biennially in a joint professionals and family workshop focusing on pediatric OMAS. Seventeen years after publication of the first report, a writing group was convened to provide a clinical update on the definitions and clinical presentation of OMAS, biomarkers and the role of investigations in a child presenting with OMAS, treatment and management strategies including identification and support of long-term sequelae. RESULTS: The clinical criteria for diagnosis were reviewed, with a proposed approach to laboratory and radiologic investigation of a child presenting with possible OMAS. The evidence for an upfront vs escalating treatment regimen was reviewed, and a treatment algorithm proposed to recognize both these approaches. Importantly, recommendations on monitoring of immunotherapy response and longer-term follow-up based on an expert consensus are provided. DISCUSSION: OMAS is a rare neurologic condition that can be associated with poor cognitive outcomes. This report proposes an approach to investigation and treatment of children presenting with OMAS, based on expert international opinion recognizing the limited data available. Lippincott Williams & Wilkins 2022-03-08 /pmc/articles/PMC8906188/ /pubmed/35260471 http://dx.doi.org/10.1212/NXI.0000000000001153 Text en Copyright © 2022 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Views & Reviews Rossor, Thomas Yeh, E. Ann Khakoo, Yasmin Angelini, Paola Hemingway, Cheryl Irani, Sarosh R. Schleiermacher, Gudrun Santosh, Paramala Lotze, Tim Dale, Russell C. Deiva, Kumaran Hero, Barbara Klein, Andrea de Alarcon, Pedro Gorman, Mark P. Mitchell, Wendy G. Lim, Ming Diagnosis and Management of Opsoclonus-Myoclonus-Ataxia Syndrome in Children: An International Perspective |
title | Diagnosis and Management of Opsoclonus-Myoclonus-Ataxia Syndrome in Children: An International Perspective |
title_full | Diagnosis and Management of Opsoclonus-Myoclonus-Ataxia Syndrome in Children: An International Perspective |
title_fullStr | Diagnosis and Management of Opsoclonus-Myoclonus-Ataxia Syndrome in Children: An International Perspective |
title_full_unstemmed | Diagnosis and Management of Opsoclonus-Myoclonus-Ataxia Syndrome in Children: An International Perspective |
title_short | Diagnosis and Management of Opsoclonus-Myoclonus-Ataxia Syndrome in Children: An International Perspective |
title_sort | diagnosis and management of opsoclonus-myoclonus-ataxia syndrome in children: an international perspective |
topic | Views & Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8906188/ https://www.ncbi.nlm.nih.gov/pubmed/35260471 http://dx.doi.org/10.1212/NXI.0000000000001153 |
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