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key points in differential diagnosis in myasthenic syndromes

dc.contributor.authorMachado, S
dc.contributor.authorPires, C
dc.contributor.authorManji, H
dc.date.accessioned2015-08-17T10:04:37Z
dc.date.available2015-08-17T10:04:37Z
dc.date.issued2013
dc.description.abstractNeuromuscular junction disorders are a heterogeneous group most often caused by imune or genetic abnormalities. They comprise Myasthenia Gravis, Lambert-Eaton Syndrome and Congenital Myasthenic Syndromes. Despite affecting different parts of the synapse, they share clinical and neurophysiological features, posing a diagnostic challenge. These disorders can be divided in subgroups, according to the causing antibody or genetic defect. However, there are no established clinical criteria and the accurate diagnosis is highly dependent on the recognition of phenotypes. The identification of clues both in the history and examination may be precious to the correct diagnosis. Treatment depends on the underlying abnormality and the prognosis is generally good. However, more severe forms of Myasthenia Gravis and paraneoplastic: Lambert-Eatom Myasthenic Syndrome are recognized.
dc.identifier.citationSinapse. 2013 Maio;13(1):15-22por
dc.identifier.issn1645-281X
dc.identifier.urihttp://hdl.handle.net/10400.10/1489
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherSociedade Portuguesa de Neurologiapor
dc.relation.publisherversionhttp://www.spneurologia.com/index.php?option=com_docman&task=doc_download&gid=79&Itemid=56por
dc.subjectCongenital myasthenic syndromespor
dc.subjectMyasthenia gravispor
dc.subjectDifferential diagnosispor
dc.subjectSíndromes miasténicos congénitospor
dc.subjectMiastenia gravispor
dc.subjectDiagnóstico diferencialpor
dc.titlekey points in differential diagnosis in myasthenic syndromespor
dc.title.alternativeAspectos fundamentais do diagnóstico diferencial dos sindromas miasténicospor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.conferencePlaceLisboapor
oaire.citation.endPage22por
oaire.citation.startPage15por
oaire.citation.titleSinapse: Publicação da Sociedade Portuguesa de Neurologiapor
oaire.citation.volume13por
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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