PAPA‐like syndrome with heterozygous mutation in the MEFV gene. (9th December 2021)
- Record Type:
- Journal Article
- Title:
- PAPA‐like syndrome with heterozygous mutation in the MEFV gene. (9th December 2021)
- Main Title:
- PAPA‐like syndrome with heterozygous mutation in the MEFV gene
- Authors:
- O'Connor, C.
Kiely, L.
Heffron, C.
Ryan, J.
Bennett, M. - Abstract:
- Abstract : 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.
- Is Part Of:
- Clinical and experimental dermatology. Volume 47:Number 3(2022)
- Journal:
- Clinical and experimental dermatology
- Issue:
- Volume 47:Number 3(2022)
- Issue Display:
- Volume 47, Issue 3 (2022)
- Year:
- 2022
- Volume:
- 47
- Issue:
- 3
- Issue Sort Value:
- 2022-0047-0003-0000
- Page Start:
- 642
- Page End:
- 645
- Publication Date:
- 2021-12-09
- Subjects:
- Skin -- Diseases -- Periodicals
616.5 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2230 ↗
https://academic.oup.com/ced/issue ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/ced.15027 ↗
- Languages:
- English
- ISSNs:
- 0307-6938
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3286.250000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 21153.xml