A Japanese family case with juvenile onset Behçet's disease caused by TNFAIP3 mutation

Allergol Int. 2017 Jan;66(1):146-148. doi: 10.1016/j.alit.2016.06.006. Epub 2016 Jul 19.

Authors

Hidenori Ohnishi¹, Norio Kawamoto², Mariko Seishima³, Osamu Ohara⁴, Toshiyuki Fukao²

Affiliations

¹ Department of Pediatrics, Gifu University Graduate School of Medicine, Gifu, Japan. Electronic address: [email protected].
² Department of Pediatrics, Gifu University Graduate School of Medicine, Gifu, Japan.
³ Department of Dermatology, Gifu University Graduate School of Medicine, Gifu, Japan.
⁴ Department of Technology Development, Kazusa DNA Research Institute, Kisarazu, Japan.

PMID: 27451268
DOI: 10.1016/j.alit.2016.06.006

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Adult
Aged
Asian People
Behcet Syndrome / genetics*
Behcet Syndrome / pathology*
Behcet Syndrome / therapy
Child
Female
Humans
Japan
Male
Mutation
Tumor Necrosis Factor alpha-Induced Protein 3 / genetics*

Substances

TNFAIP3 protein, human
Tumor Necrosis Factor alpha-Induced Protein 3