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Last weekend, 27-28 October 2012, the meeting on 1st European Days of Albinism, was held in Paris (France), hosted by the French Platform of Rare Diseases and organized by Genespoir, the French association in support of persons with albinism. This meeting was co-sponsored by the European Society for Pigment Cell Research (ESPCR).
About 65 participants, representing various associations on albinism from various countries (France, Spain, Italy, Germany, Netherldans, UK and Ireland, Denmark, Norway) and scientists (ophthalmologists, geneticists, dermatologists, molecular biologists) gathered in Paris to discuss various aspects around albinism, from the latest research on genetics, animal models, diagnosis and therapeutic interventions, to the common problems, needs and demands faced by persons with albinism and their families.











