SCN8A France

SCN8A France

Pierrevert, France

HealthMedical research
AssociationFounded 2021National reach
Profile last updated: March 15, 2026

About

Founded in 2021, SCN8A France is a non-profit association based in Pierrevert, France working on health, medical research.

SCN8A France is a French patient association created in November 2021 by a group of parents. It supports families affected by SCN8A-related disorders, a rare genetic condition caused by mutations in the SCN8A gene. The association shares information about the condition, offers mutual support and peer exchange for families, provides practical guidance on administrative and financial aid, lends adapted equipment, and advocates for recognition and research progress with public authorities, laboratories and specialist networks. It is a member of Alliance Maladies Rares and EFAPPE and is part of the European SCN8A Foundation.

Location

Pierrevert, France

Founded

2021

Organisation type

Association

Focus areas

SCN8Arare diseaseepilepsygenetic disorderpatient associationfamily support

Languages

FR

Causes & programmes

Causes

HealthMedical research

Works for

PatientsFamiliesCarers

How they work

Awareness & educationAdvocacy & campaigningCommunity programmes

Countries of operation

France

Funding & support

Funded by

Individual donations

Ways to support

DonateVolunteerMembership

Credentials & affiliations

Industry memberships

Alliance Maladies RaresEFAPPE

Partnerships

Défiscience, Fondation Européenne SCN8A

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