top of page
Who we are
The European KCNQ2 Association (EKA) was born from the collaboration of seven Italian members, mothers and fathers of children carrying the KCNQ2 genetic modification and / or suffering from rare epilepsies, with the aim of becoming the reference point in Europe in support of projects research and to support initiatives and information for families.

Alessandra Costa Cosciani
President

Elisa Remonato
Vice president

Sara Gramaglia
Secretary

Anna Accomando
Partner-Founder

Roberta Brazzale
Partner-Founder

Peter Franz Dorigotti
Partner-Founder

Isabella Brambilla
Partner-Founder
bottom of page