Primary hypertrophic osteoarthropathy with severe arthralgia identified by gene mutation of SLCO2A1-Reference-Cited by-同舟云学术

Primary hypertrophic osteoarthropathy with severe arthralgia identified by gene mutation of SLCO2A1

Published:2021-01-18 Issue:2 Volume:5 Page:404-408
ISSN:2472-5625
Container-title:Modern Rheumatology Case Reports
language:en
Short-container-title:Modern Rheumatology Case Reports

Author:

Ishizuka Tatsuo¹,Fujioka Kei¹,Mori Ichiro¹,Takeda Tomofumi¹,Fuwa Masayuki¹,Ikeda Takahide²,Taguchi Koichiro²,Morita Hiroyuki²,Nakabayashi Kazuhiko³⁴,Niizeki Hironori³⁴

Affiliation:

1. Center of General Internal Medicine and Rheumatology, Gifu Municipal Hospital, Gifu, Japan

2. Department of General Internal Medicine, Gifu University Graduate School of Medicine, Gifu, Japan

3. Department of Maternal-Fetal Biology, National Center for Child Health and Development, Tokyo, Japan

4. Department of Dermatology, National Center for Child Health and Development, Tokyo, Japan

Publisher

Oxford University Press (OUP)

Subject

General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/24725625.2020.1861744

Reference14 articles.

1. Involvement of prostaglandin E2 in the first Japanese case of pachydermoperiostosis with HPGD mutation and recalcitrant leg ulcer

2. Mutations in 15-hydroxyprostaglandin dehydrogenase cause primary hypertrophic osteoarthropathy

3. A Hereditary Enteropathy Caused by Mutations in the SLCO2A1 Gene, Encoding a Prostaglandin Transporter

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