Phelan-McDermid Syndrome Association
The Phelan-McDermid Syndrome Association, based in Madrid, Spain, is composed of parents and relatives of the persons affected by this rare disease. It was created in 2013 and was classified as an Entity of Public Interest in 2016.
We aim at improving the quality of life of people affected by the syndrome by accelerating research, supporting families and raising awareness. Through our organization in Spain, we offer reliable and up-to-date information about the syndrome, a community of support for families and we seek funding to support research about the syndrome.
