Update on Ocular Myasthenia Gravis

Autor: Meabh O'Hare, Christopher T. Doughty
Rok vydání: 2019
Předmět:
Zdroj: Seminars in Neurology. 39:749-760
ISSN: 1098-9021
0271-8235
DOI: 10.1055/s-0039-1700527
Popis: Myasthenia gravis is an antibody-mediated autoimmune disorder of the post-synaptic neuromuscular junction resulting in fluctuating, fatigable weakness. Most patients first present with extraocular symptoms (diplopia and/or ptosis), and in 15% of cases symptoms will remain restricted to only the extraocular muscles (ocular myasthenia gravis [OMG]). The history and clinical examination are of the utmost importance in correctly identifying OMG patients, as supportive serologic or electrodiagnostic studies are frequently nondiagnostic. In this review, we outline a diagnostic approach to OMG (focusing on key clinical features), discuss therapeutic options, and highlight recent developments in the understanding of OMG.
Databáze: OpenAIRE