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. 2021 Nov;76(11):3529-3534.
doi: 10.1111/all.15034. Epub 2021 Aug 12.

Clinical and genetic features of hereditary angioedema with and without C1-inhibitor (C1-INH) deficiency in Japan

Chinami Hashimura  1   2 , Chikako Kiyohara  3 , Jun-Ichi Fukushi  1 , Tomoya Hirose  2   4 , Isao Ohsawa  5 , Tomoko Tahira  6 , Takahiko Horiuchi  2   7
Affiliations

Clinical and genetic features of hereditary angioedema with and without C1-inhibitor (C1-INH) deficiency in Japan

Chinami Hashimura et al. Allergy. 2021 Nov.
No abstract available

Keywords: Japanese; factor XII; hereditary angioedema; hereditary angioedema with normal C1-inhibitor; plasminogen.

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Conflict of interest statement

As for COI, Dr. Hashimura has nothing to disclose. Dr. Kiyohara has nothing to disclose. Dr. Fukushi has nothing to disclose. Dr. Hirose is a consultant for Takeda Pharmaceutical Company (without salary). Dr. Ohsawa reports personal fees from Takeda Pharmaceutical Company, personal fees from CSL Behring, personal fees from Torii Pharmaceutical Company, personal fees from BioCryst Pharmaceuticals, outside the submitted work. Dr. Tahira has nothing to disclose. Dr. Horiuchi reports personal fees from Takeda Pharmaceutical Company, personal fees from CSL Behring, personal fees from Torii Pharmaceutical Company, outside the submitted work.

References

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    1. Yakushiji H, Hashimura C, Fukuoka K, et al. A missense mutation of the plasminogen gene in hereditary angioedema with normal C1 inhibitor in Japan. Allergy. 2018;73(11):2244‐2247. - PubMed

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