par Rasquin, Florence ;Van Nechel, Christian ;Cordonnier, Monique
Référence Bulletin de la Société belge d'ophtalmologie, 313, page (9-12)
Publication Publié, 2009
Article révisé par les pairs
Résumé : To document for the first time intrinsic retinal pigment epithelium (RPE) fluorescence in occult macular dystrophy (OMD). This entity is characterized by a central cone dysfunction leading to a decline of visual acuity without visible fundus and fluorescein angiography abnormalities. A great variability in clinical findings and in the pattern of inheritance have been reported suggesting probably several etiologies of which some are well known but seen too early to detect significant changes.