1.
Artículo
en Inglés
| IMSEAR
| ID: sea-177091
RESUMEN
Myasthenia gravis (MG) is an autoimmune disorder of the neuromuscular junction of skeletal muscles. Patients affected with MG may present with ocular features or develop ocular involvement later in the course of the disease, known as ocular MG (OMG). OMG can mimic ptosis, commitant and incommitant strabismus, cranial nerve palsies, gaze palsies and internuclear ophthalmoplegia. Hence, it is important to establish a correct diagnosis and start appropriate treatment. This review focuses on the clinical features, diagnosis, and management of OMG.