par Abeloos, M C;Cordonnier, Monique ;Van Nechel, Christian ;Van Bogaert, Patrick ;Gérard, Jean-Marie;Van Regemorter, Nicole
Référence Bulletin de la Société belge d'ophtalmologie, 239, page (61-74)
Publication Publié, 1990
Article révisé par les pairs
Résumé : 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.

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