MeSH Browser

MeSH Supplementary: Pyogenic arthritis, pyoderma gangrenosum, and acne
Unique ID: C536253
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536253
Entry Term(s): Familial recurrent arthritis; PAPA syndrome; Pyogenic Sterile Arthritis, Pyoderma Gangrenosum, and Acne; Pyogenic arthritis, pyoderma gangrenosum, and severe cystic acne
Heading Mapped to: *Acne Vulgaris; *Arthritis, Infectious; *Pyoderma Gangrenosum
Frequency: 61
Note: A hereditary autosomal dominant disorder characterized by pyogenic (infectious) arthritis, pyoderma gangrenosum, and severe cystic acne. Onset is in childhood; pyoderma gangrenosum; and severe cystic acne occur in adolescence and beyond. Other less common features may include adult-onset DIABETES MELLITUS, TYPE I; PROTEINURIA, ABSCESS formation at the site of parenteral injections, and cytopenias attributable to SULFONAMIDE medications. Mutations in the PSTPIP1 gene have been identified. OMIM: 604416
Date of Entry: 2010/08/25
Revision Date: 2015/08/18

Pyogenic arthritis, pyoderma gangrenosum, and acne MeSH Supplementary Concept Data 2024