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Update on Ocular Myasthenia Gravis.
Smith, Stacy V; Lee, Andrew G.
Afiliação
  • Smith SV; Department of Ophthalmology, Blanton Eye Institute, Houston Methodist Hospital, Scurlock Tower, 6560 Fannin Street, Suite 450, Houston, TX 77030, USA.
  • Lee AG; Department of Ophthalmology, Blanton Eye Institute, Houston Methodist Hospital, Scurlock Tower, 6560 Fannin Street, Suite 450, Houston, TX 77030, USA; Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA; Department of Ophthalmology, University of Texas Medical Branch (UTMB), Galveston, TX, USA; Department of Ophthalmology, Weill Cornell Medicine, New York, NY, USA; Department of Neurology, Weill Cornell Medicine, New York, NY, USA; Department of Neurosurgery, Weill Cornell Medicin
Neurol Clin ; 35(1): 115-123, 2017 02.
Article em En | MEDLINE | ID: mdl-27886889
ABSTRACT
Ocular myasthenia gravis (OMG) is a localized form of myasthenia gravis in which autoantibodies directed against acetylcholine receptors block or destroy these receptors at the postsynaptic neuromuscular junction. The hallmark of OMG is a history of painless weakness or fatigability of the extraocular muscles and ptosis with normal pupillary function and visual acuity. Clinical, laboratory, electrophysiologic, and pharmacologic tests are available for diagnosis. Treatment can begin with symptom management; there is no cure. Prognosis is improved by use of immunomodulators. Despite advances in treatment, research is needed, especially in the areas of surgical intervention and medical therapy based on risk stratification.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Miastenia Gravis Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Miastenia Gravis Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article