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Pachyonychia Congenitia Project

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

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PC & Children

PC Project is here to help kids navigate a tough, rare condition.

I was born a healthy, normal baby. At 5 days old my nails were a deep yellow. – Coraline

Welcome to our special kids’ section: The PC Kids Corner! This section is all about your PC and growing up with PC and was made possible in part by a grant from Jeans for Genes to Pachyonychia Congenita Project Europe.

Having PC is not always easy, but we promise that you can still have a happy successful life, even with PC. We hope that as children or teenagers with PC, along with your parents or caregivers, you will use this part of the website to learn valuable information about your condition.

While the main PC website contains much of what you need to know about PC and living with PC, the information provided here is to give you ‘bite’ sized pieces of information which are hopefully easy for you to understand. 

(Although this part of our webpage is primarily aimed at children and teenagers, parents and caregivers may find the information helpful.)

If there is information you think we should include in this page for PC kids, please let us know at info@pachyonychia.org.

Next Section: What is PC?

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  • PC & Children
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    • Supporting PC Project and the PC Community
    • Brilliant things kids with PC are achieving!

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PACHYONYCHIA CONGENITA PROJECT

P.O. Box 17850
Holladay, UT 84117

info@pachyonychia.org

801-987-8758

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