International Pachyonychia Congenita Research Registry

Description

International Pachyonychia Congenita Research Registry (IPCRR) is a patient registry for those suffering from Pachyonychia Congenita (PC). PC is an ultra-rare extremely painful skin disorder that causes painful blisters and callus on feet and sometimes hands, thickened nails, cysts and other features. The IPCRR consists of a questionnaire, patient photos, optional physician notes from telephone consultation to validate questionnaire and free genetic testing.

Conditions

Pachyonychia Congenita

Study Overview

Study Details

Study overview

International Pachyonychia Congenita Research Registry (IPCRR) is a patient registry for those suffering from Pachyonychia Congenita (PC). PC is an ultra-rare extremely painful skin disorder that causes painful blisters and callus on feet and sometimes hands, thickened nails, cysts and other features. The IPCRR consists of a questionnaire, patient photos, optional physician notes from telephone consultation to validate questionnaire and free genetic testing.

International Pachyonychia Congenita Research Registry

International Pachyonychia Congenita Research Registry

Condition
Pachyonychia Congenita
Intervention / Treatment

-

Contacts and Locations

Salt Lake City

Pachyonychia Congenita Project, Salt Lake City, Utah, United States, 84117

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Clinical diagnosis of Pachyonychia Congenita or similar disorder
  • * N/A

Ages Eligible for Study

to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

Pachyonychia Congenita Project,

C. David Hansen, MD, PRINCIPAL_INVESTIGATOR, Pachyonychia Congenita Project

Study Record Dates

2030-12