Congenital fibrosis of thr ocular muscles: a diagnosis for several clinical pictures
Abeloos, M.C.; Cordonnier, M.; Van Nechel, C.; Van Bogaert, P.; Gerard, J.M.; Van Regemoorter, N.
Bulletin de la Societe Belge d'Ophtalmologie 239: 61-74
1990
ISSN/ISBN: 0081-0746 PMID: 2133536 Document Number: 355099
Case report of four members of a family presenting a congenital fibrosis syndrome. The first case has the typical presentation with bilateral ptosis, bilateral hypotrophic, variable horizontal deviation, and restricted ocular movements in all directions. The second case has a unilateral ptosis with Marcus Gunn phenomenon and bilateral restriction of elevation. In the third case, the condition is purely unilateral and associated with a sensorimotor neuropathy. A fourth member presents a unilateral ptosis. Three other members have a simple strabismus without any oculomotor anomaly.