PAPA-like syndrome with heterozygous mutation in the MEFV gene

Autor:	C. O’Connor, L. Kiely, C. Heffron, J. Ryan, M. Bennett
Rok vydání:	2021
Předmět:	Adult Male Arthritis Infectious Dermatology Syndrome Pyrin Pyoderma Gangrenosum Tubulin Modulators Cicatrix Muscular Atrophy Recurrence Acne Vulgaris Mutation Humans Colchicine
Zdroj:	Clinical and experimental dermatologyReferences. 47(3)
ISSN:	1365-2230
Popis:	A patient presented with a history of recurrent pyoderma gangrenosum, arthritis and extensive acne, prompting a genetic workup for PAPA syndrome. An MEFV mutation was identified and a change in therapeutic strategy from anakinra to colchicine was successful. Click https://www.wileyhealthlearning.com/#/online-courses/b52447c0-1d37-472d-b0c0-7817352d6f68 for the corresponding questions to this CME article.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a6beed039bbf29c4b829a0810336e1d https://pubmed.ncbi.nlm.nih.gov/34882829 Zobrazit plný text záznamu Plný text