Our Mission:
To transform the uncertainty and isolation of a rare genetic diagnosis into organization, scientific knowledge, and collective action. We are dedicated to raising awareness, accelerating access to early genetic diagnoses, fostering clinical research, and preparing our local community to participate in future clinical trials that will lead to effective targeted therapies and a cure.
Contact us:
Contact us at info@syngap1.com.ar or fundacionsyngap1ar@gmail.com
Valeria Torcetta (President): +54 9 11 3111-5064
Fernanda Caparros (Vice President): +54 9 11 3118-2420
Visit our website at syngap1.com.ar
Organization Leaders
Number of Known Patients in Argentina – 24
See the latest SYNGAP1 Census for all details!
