The “PROGETTO MITOFUSINA 2 ONLUS” association was founded on August 28th, 2012 by a group of parents, relatives and friends of adult and child patients affected by a very rare disease: peripheral hereditary neuropathy caused by Mitofusin 2 gene (MFN2) mutation.
This non-profit association aims to create a network for Italian and foreign families of patients affected by CMT2A, as well as to promote collaboration with researchers and medical professionals and to raise funds for the development of scientific research on CMT2A. Also, the association is committed to organise and promote events, conferences and meetings to raise awareness on this rare disease.
CONTACTSHEAD OFFICE: Via Maria Montessori 9, 50067 Rignano sull’Arno (Firenze)
Eleonora Bartolini - PRESIDENT
Via Montessori 9 - 50067 Rignano sull’Arno (FI)
Luisa Perrero Porzio – TURIN REPRESENTATIVE