Sm. Lee et al., CONGENITAL FIBROSIS SYNDROME - ULTRASTRUCTURAL AND ELECTRONYSTAGMOGRAPHIC STUDY, Annals of ophthalmology. Glaucoma, 30(5), 1998, pp. 282-285
Congenital fibrosis syndrome is inherited autosomal-dominantly and exh
ibited in infancy as blepharoptosis, fixed hypodeviation of both eyes,
chin elevation, and convergence nystagmus on attempted gaze. We repor
t 3 cases of congenital fibrosis syndrome! in a family with characteri
stic features. This article discusses the results of radiologic examin
ation of the patients' central nervous system and the pathophysiologic
mechanism of these nystagmoid movements.