Hereditary angioedema: Report of a case
Publication in refereed journal


香港中文大学研究人员 ( 现职)

Professor Gavin Matthew JOYNT (麻醉及深切治疗学系)

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摘要Hereditary angioedema is caused by an absolute deficiency or the functional inactivity of C1 esterase inhibitor in plasma. A precise diagnosis is important because, unlike allergic forms of mucocutaneous edema, this condition does not respond to epinephrine, antihistamines, or corticosteroids. We report the case of a 24-year-old man who experienced an acute attack after he had stopped taking his prophylactic medication.

着者Joynt G.M., Abdullah V., Wormald P.J.
期刊名称Ear Nose and Throat Journal
出版年份2http://aims.cuhk.edu.hk/converis/portal/Publication/0http://aims.cuhk.edu.hk/converis/portal/Publication/01
月份11
日期2http://aims.cuhk.edu.hk/converis/portal/Publication/0
卷号8http://aims.cuhk.edu.hk/converis/portal/Publication/0
期次5
出版社Medquest Communications
出版地United States
页次321 - 324
国际标準期刊号http://aims.cuhk.edu.hk/converis/portal/Publication/0145-5613
电子国际标準期刊号1942-7522
语言英式英语