Skip to main content
Skip to footer

Pachyonychia Congenitia Project

Fighting for a cure. Connecting & helping patients. Empowering Research.

VIEW MENUMENU

Pachyonychia Congenita
For Professionals
Ways To Give
- - - Ways You Can Give
  - - Raise Awareness
News & Events
- - - News
  - - Events
About Us

Keratin 13 point mutation underlies the hereditary mucosal epithelial disorder white sponge nevus

November 1, 2016 by

Footer

PACHYONYCHIA CONGENITA PROJECT

P.O. Box 17850
Holladay, UT 84117

info@pachyonychia.org

801-987-8758

Sign up for our Newsletter

Name *

First

Last

Email *

Tell us about yourself

Support PC Project

There are many ways you can help improve the lives of those who suffer from Pachyonychia Congenita.

Contact Us
About Us
Donate
Patient Registry

Copyright © 2023 PC Project. All rights reserved. Pachyonychia Congenita Project is a 501(c)(3) under federal tax guidelines. Using this site means you accept its terms as outlined in the disclaimer and privacy policy.