RESEARCH AND COMPARISONS 2020 -A DECISIVE TURNING POINT-

Our HISTORY is at a truly decisive moment as p63 and the syndromes caused by protein alteration, and in particular the EEC and AEC syndrome, are presented in an exclusive webinar whose objectives are the valorisation of research and scientific knowledge for the care of patients. RESEARCH AND COMPARISON 2020 wishes to provide new opportunities and combine both scientific knowledge of the p63 gene and the orientation of the patient's clinical and surgical care in order to ensure a good quality of life.
Whatever your role in the sphere of rare diseases, RESEARCH and COMPARISON will be the platform that will have a great impact thanks to the collaboration of eminent REPORTERS and the direct involvement of patients from all over the world. The language of rare disease patients is now understandable to all as a result of the Covid-19 health emergency and the physical and social distance it has brought in a pandemic way.

In 2013 and 2015, we provided the first opportunities to build an international network bringing together opinions and stakeholders from around the world. The RESEARCH and COMPARISON 2020 webinar on 26 and 27 November 2020 will provide multiple opportunities to finally gather all the stakeholders involved in the sector. Among them, we would particularly like to thank MIUR, UNIPD, TELETHON, I.S.S, ERN SKIN, EURORDIS and UNIAMO for successfully bringing together the Italian associations.
Important progress has been made towards a concrete future and the presentation of the latest surgical technologies of the new genetic therapies, all of which will be accessible to the members of the webinar in order to discover the different workstreams and innovations in this field.