Abstract
Lambert-Eaton myasthenic syndrome is a rare and acquired autoimmune disorder. We describe two female patients with medial rectus paresis as the only ocular manifestation. After a unilateral medial rectus recession and lateral rectus resection procedure, both patients recovered normal adduction. To our knowledge, this is the first report of surgery for extraocular muscle paresis in Lambert-Eaton myasthenic syndrome.
Cite
CITATION STYLE
Krieger, F. T., & Goldchmit, M. (2009). Surgical correction of strabismus in Lambert-Eaton myasthenic syndrome: case reports. Arquivos Brasileiros de Oftalmologia, 72(1), 99–102. https://doi.org/10.1590/s0004-27492009000100020
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.