Background: Gyrate atrophy of the retina and choroid is a rare disease, with recessive autosomal transmission, characterized by progressive chorioretinal atrophy causing blindness. It results from a congenital deficit in aminotransferase ornithine.
Case Report: The authors present the case of a young patient aged 15 years old consulting for a progressive fall of visual acuity with hemeralopia.
Purpose: To evaluate visual outcome after epiretinal membrane surgery.
Material: and method: Retrospective study of 50 consecutive epiretinal membranes (ERM) (23 idiopathic and 27 secondary) with 12 to 42-month follow-up (mean 24 months). Functional evaluations were performed before and after surgery according to the idiopathic or secondary nature of the epiretinal membranes.
We report a case of Goldenhar syndrom in thirty eight old woman who has been refered to us for peribulbar choristoma. The authors discuss the different ophthalmological, otolaryngological and general manifestation of this syndrom and the therapeutic modalities of the ocular anomalies.
View Article and Find Full Text PDFSince the beginning of the 80s, Montréal's population of non French--and non English-speaking inhabitants has increased rapidly, especially in schools (estimates show that by the year 2000, this segment will represent about 50% of students). In addition, this population of diverse origins is composed of only a minority of Europeans; Caribbeans and Orientals make up the vast majority of immigrants that have settled in Montréal over the last decade. How does this unique mix of cultural backgrounds impact on the perception that these youth from multiethnic neighbourhoods have of their own culture and social relations? This is the basic issue that the authors have attempted to solve in the course of their research.
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