Overview For PC Patients
The Video Archive has dozens of presentations on a variety of topics related to PC. Click Here to select a topic of interest.
Click the link above for News and Events as well as copies of all PC Patient NewsBrief issues and IPCC Newsletters.
IPCRR Patient Registry Data
Patients in the IPCRR are helping physicians and scientists discover more about PC. This research is leading to the develoopment of treatments for PC. Data from the IPCRR patient registry is available on the PC Data tab including the location of PC patients by country and state, listings of all of the genes and mutations linked to Pachyonychia Congenita, a summary of the registry data and other helpful charts and graphs.
Join the Patient Registry or update your information
Focus on PC Patients
The many parts and pieces of this new website are designed to empower and educate patients by providing accurate up-to-date information as well as support. We want to give hope knowing that many leading scientists around the world are collaborating in this quest to develop effective treatments for the ultra rare disorder known as Pachyonychia Congenita.
We invite you to visit the website often to read new patient stories, to check on events and news, to access recent publications and learn of new developments. Explore the entire website, which is designed as a resource to provide easy access to information on Pachyonychia Congenita for you, for your family and friends, and for professionals who may be providing care.