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

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

Chinami Hashimura^{1

2}, Chikako Kiyohara³, Jun-Ichi Fukushi¹, Tomoya Hirose^{2

4}, Isao Ohsawa⁵, Tomoko Tahira⁶, Takahiko Horiuchi^{2

7}

¹ Clinical Research Center, National Hospital Organization Kyushu Medical Center, Fukuoka, Japan.
² Center for Research, Education, and Treatment of angioEdema, a specified Non-profit Corporation, Fukuoka, Japan.
³ Department of Preventive Medicine, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
⁴ Department of Traumatology and Acute Critical Medicine, Osaka University Graduate School of Medicine, Osaka, Japan.
⁵ Department of Nephrology, Internal Medicine, Saiyu Soka Hospital, Saitama, Japan.
⁶ College of Pharmacy, Kinjo Gakuin University, Nagoya, Japan.
⁷ Department of Internal Medicine, Kyushu University Beppu Hospital, Oita, Japan.

No abstract available

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

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