PSORIASIS AND PSORIATIC ARTHRITIS RESEARCH REGISTRY

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This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. The investigators wish to establish a registry of patients with psoriasis and psoriatic arthritis. Participants will be asked to sign informed consent, which will allow the collection of data (standard of care lab results and X-rays, as well as a questionnaire) both prospective and retrospective in nature and a physical exam. Some blood will be collected for storage. Encounters will be made 2-4 times a year. Patients (>18 years of age) will be enrolled at HJD and by referral from private doctors in serial fashion. Enrollment of 100 is planned.