Rare genetic neurodevelopmental disorders are often associated with autism spectrum disorder (ASD). For example, about 30% of individuals with Fragile… Read more »
Dr. Ségolène Aymé is the Editor-in-Chief for Orphanet Journal of Rare Diseases. She is the founder of Orphanet, and chair of the Topic Advisory… Read more »
Today is Rare Disease Day, aiming to make the voice of rare diseases heard. Here we’ve put together some questions intended to… Read more »
Earlier this year, Findacure, in conjunction with Orphanet Journal of Rare Diseases, announced the winner of its student essay… Read more »
Earlier this year, Findacure, in conjunction with Orphanet Journal of Rare Diseases, announced the winner of its student essay… Read more »