At DupMECP2 Family Support Fund Now Open Nous savons que s’occuper d’un enfant atteint du syndrome de duplication du gène MECP2 implique souvent bien plus que de Read more » July 8, 2026
At DupMECP2 Renew your membership: make 2025 a special year for DupMECP2 Written by Bruna In 2024, over 200 members joined us to raise awareness of the syndrome. We are Read more » January 18, 2025
At DupMECP2 Meet our new team members At the end of 2024, we welcomed two new members to the team: Klaus Salentin from Germany, who lives in Thailand, Read more » January 4, 2025