Dermatomyositis‐like eruptions and fasciitis with novel compound heterozygous MEFV mutations: Newly recognized features of a variant of familial Mediterranean fever-Reference-Cited by-同舟云学术

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Dermatomyositis‐like eruptions and fasciitis with novel compound heterozygous MEFV mutations: Newly recognized features of a variant of familial Mediterranean fever

Published:2021-06-17 Issue:9 Volume:48 Page:1453-1456
ISSN:0385-2407
Container-title:The Journal of Dermatology
language:en
Short-container-title:J Dermatol

Author:

Sumida Hayakazu¹^ORCID,Migita Kiyoshi²,Ida Hiroaki³,Asano Yoshihide¹^ORCID,Shimizu Jun⁴,Kagami Shinji¹^ORCID,Sugaya Makoto¹^ORCID,Kadono Takafumi¹,Sato Shinichi¹

Affiliation:

1. Department of Dermatology Faculty of Medicine The University of Tokyo Tokyo Japan

2. Department of Rheumatology School of Medicine Fukushima Medical University Fukushima Japan

3. Division of Respirology, Neurology, and Rheumatology Department of Medicine Kurume University School of Medicine Kurume Japan

4. Department of Neurology Graduate School of Medicine The University of Tokyo Tokyo Japan

Publisher

Wiley

Subject

Dermatology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/1346-8138.16031

Reference18 articles.

1. Criteria for the diagnosis of familial mediterranean fever

2. MEFV mutations in patients with familial Mediterranean fever in the Black Sea region of Turkey: Samsun experience [corrected];Yigit S;J Rheumatol,2008

3. Familial Mediterranean fever—A review

4. Preliminary criteria for classification of adult Still's disease;Yamaguchi M;J Rheumatol,1992

5. Successful treatment using tacrolimus (FK506) in a patient with TNF receptor-associated periodic syndrome (TRAPS) complicated by monocytic fasciitis

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