Hereditary Angioedema: Three Cases Report, Members of the Same Family

eJournal of Oral Maxillofacial Research

article

Mattheos Papamanthos¹  Apostolos Matiakis²  Paraskevi Tsirevelou³  Alexandros Kolokotronis⁴  Haralambos Skoulakis³ 

[1] Department of Dentistry, General Hospital of Volos;Department of Internal Medicine, General Hospital AHEPA, School of Medicine, Aristotelian University of Thessaloniki;Department of Otorinolaryngology, General Hospital of Volos;Department of Oral Medicine and Maxillofacial Pathology, School of Dentistry, Aristotelian University of Thessaloniki

关键词: hereditary angioedema;    laryngeal edema;    oral surgical procedure;    operative dentistry;    tooth extraction;   

DOI  :  10.5037/jomr.2010.1109

学科分类：社会科学、人文和艺术（综合）

来源: Stilus Optimus

【 摘 要 】

This current clinical case report highlights three cases of Hereditary angioedema (HAE) patients who are all members of the same family (father and his two daughters). The father has C1–INH deficiency, while his daughters have low C1–INH levels: the first possesses only 10% function and the second has low C1–INH level with 0% function. Of note, the second daughter was discovered to have HAE at the age of 2, thus making her the youngest known HAE case report in the English literature.

【 授权许可】

CC BY-NC-ND