Our association was officially born in July 2021, we are a group of parents of children and young people with mutations in the STXBP1 gene, to date we have reached 30 families but we know that there are many more diagnoses in Italy.

Together we have formed the association “STXBP1 ITALIA”, created to protect the social rights, civil life and to promote autonomy and improvement of life quality in people affected by alteration of the STXBP1 gene and their families. We wish to promote social inclusion and  with the help of a Scientific Committee, we wish to promote and support research in order to find therapies and therapeutic paths accessible to all.

Get in contact with us:

Website: stxbp1.it

e-mail: segreteria@stxbp1.it