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FOSMN: the facial expression of ALS

dc.contributor.authorCarvalho, Mamede
dc.date.accessioned2022-09-09T11:03:22Z
dc.date.available2022-09-09T11:03:22Z
dc.date.issued2022
dc.description© 2022 International Federation of Clinical Neurophysiology. Published by Elsevier B.V. All rights reserved.pt_PT
dc.description.abstractFacial onset sensory and motor neuronopathy (FOSMN syndrome) was described as a new neurological condition 16 years ago, in a study including 4 patients (Vucic et al., 2006). The disease was characterized by sensory changes in the face, chest and arms, associated with progressive weakness in the bulbar region, neck and upper limbs, and fasciculations. Nerve conduction studies disclosed low sensory nerve action potential (SNAP) amplitudes in upper limbs, and needle EMG confirmed neurogenic signs in bulbar and cervical anatomical regions. The suspected neurodegenerative origin was supported by the loss of lower motor neurons in the hypoglossal nucleus and cervical anterior horns, and the loss of sensory neurons in the dorsal root ganglia and trigeminal sensory nucleus in the post-mortem study of one of the included patient. In another study with 4 patients, including one woman, the authors proposed a link to amyotrophic lateral sclerosis (ALS), since one patient progressed to respiratory failure and another had neurogenic motor unit potentials in muscles innervated by the spinal cord lumbar region (Fluchere et al., 2011).pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationClinical Neurophysiology 140 (2022) 167-168pt_PT
dc.identifier.doi10.1016/j.clinph.2022.05.007pt_PT
dc.identifier.eissn1872-8952
dc.identifier.issn1388-2457
dc.identifier.urihttp://hdl.handle.net/10451/54402
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherElsevierpt_PT
dc.relation.publisherversionhttps://www.journals.elsevier.com/clinical-neurophysiologypt_PT
dc.titleFOSMN: the facial expression of ALSpt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage168pt_PT
oaire.citation.startPage167pt_PT
oaire.citation.titleClinical Neurophysiologypt_PT
oaire.citation.volume140pt_PT
person.familyNamede Carvalho
person.givenNameMamede
person.identifier.orcid0000-0001-7556-0158
person.identifier.scopus-author-id7101893769
rcaap.rightsrestrictedAccesspt_PT
rcaap.typearticlept_PT
relation.isAuthorOfPublicationdd7f55d4-c2b5-4fd2-9bd1-a9542a62f58f
relation.isAuthorOfPublication.latestForDiscoverydd7f55d4-c2b5-4fd2-9bd1-a9542a62f58f

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