
Our Mission:
The “Together for SYNGAP1” Association supports children and adults affected by SYNGAP1 gene mutations and other rare diseases. The organization works to raise awareness about SYNGAP1, support families, improve patients’ quality of life, and promote the development of diagnostics, therapies, and scientific research related to this rare condition. The association collaborates with doctors, therapists, and international organizations; organizes educational and community events; and helps families access appropriate care and therapy.
Contact us:
Contact us at kontakt@syngap1.com.pl
Visit our website at https://syngap1.com.pl/
Organization Leaders



Number of Known Patients in Poland – 53
See the latest SYNGAP1 Census for all details!


