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September 2021

EUROPE SCN8A & SCN2A CONFERENCE & FAMILY GATHERING

September 10 - September 11

WELCOME TO EUROPE'S FIRST SCN8A & SCN2A CONFERENCE & FAMILY GATHERING BUILDING A NETWORK ACROSS EUROPE AND BEYOND. SCN8A and SCN2A related diseases are extremely rare, likely under diagnosed, neurodevelopmental disorders caused by variants to the SCN2A / SCN8A genes. While sharing similarities with better known Dravet Syndrome (SCN1A), SCN8A/2A are different and can require different treatment. Improved awareness and early diagnosis are key. SCN2A & SCN8A also have differences, but as rare sodium-channel disorders there is commonality of research…

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