Publication:
Diagnosis and Management of Opsoclonus-Myoclonus-Ataxia Syndrome in Children: An International Perspective.

cris.virtualsource.author-orcidec07bc23-df49-4df8-b0e5-3ab649762c82
datacite.rightsopen.access
dc.contributor.authorRossor, Thomas
dc.contributor.authorYeh, E Ann
dc.contributor.authorKhakoo, Yasmin
dc.contributor.authorAngelini, Paola
dc.contributor.authorHemingway, Cheryl
dc.contributor.authorIrani, Sarosh R
dc.contributor.authorSchleiermacher, Gudrun
dc.contributor.authorSantosh, Paramala
dc.contributor.authorLotze, Tim
dc.contributor.authorDale, Russell C
dc.contributor.authorDeiva, Kumaran
dc.contributor.authorHero, Barbara
dc.contributor.authorKlein, Andrea Katharina
dc.contributor.authorde Alarcon, Pedro
dc.contributor.authorGorman, Mark P
dc.contributor.authorMitchell, Wendy G
dc.contributor.authorLim, Ming
dc.date.accessioned2024-10-09T17:10:42Z
dc.date.available2024-10-09T17:10:42Z
dc.date.issued2022-05-08
dc.description.abstractBACKGROUND 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.
dc.description.sponsorshipUniversitätsklinik für Kinderheilkunde
dc.identifier.doi10.48350/167240
dc.identifier.pmid35260471
dc.identifier.publisherDOI10.1212/NXI.0000000000001153
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/68692
dc.language.isoen
dc.publisherWolters Kluwer Health
dc.relation.ispartofNeurology: Neuroimmunology and Neuroinflammation
dc.relation.issn2332-7812
dc.relation.organizationDCD5A442BB6FE17DE0405C82790C4DE2
dc.relation.organizationDCD5A442BADAE17DE0405C82790C4DE2
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titleDiagnosis and Management of Opsoclonus-Myoclonus-Ataxia Syndrome in Children: An International Perspective.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.issue3
oaire.citation.volume9
oairecerif.author.affiliationUniversitätsklinik für Kinderheilkunde
oairecerif.author.affiliation2Universitätsklinik für Kinderheilkunde, Neuropädiatrie
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unibe.date.licenseChanged2022-03-13 05:09:11
unibe.description.ispublishedpub
unibe.eprints.legacyId167240
unibe.refereedtrue
unibe.subtype.articlereview

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