Hereditary angioedema with F12 mutation: first report of three cases associated with immune disorders.
نویسندگان
چکیده
منابع مشابه
Report on the First Survey of Iranian Patients with Hereditary Angioedema
Background: Hereditary angioedema (HAE) is a rare autosomal dominant primary immunodeficiency with complement system defect characterized by recurrent episodes of angioedema involving the skin or mucosa of the upper respiratory and gastrointestinal tracts. Objective: To characterize the clinical and laboratory data of hereditary angioedema in Iran. Methods: Patients with probable diagnosis of a...
متن کاملHereditary Angioedema: Three Cases Report, Members of the Same Family
BACKGROUND 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 h...
متن کاملMandibular First Molar with Five Canals: A Report of Three Cases
The main objective of endodontic therapy is the thorough mechanical and chemical cleansing of the entire root canal system and its complete obturation with an inert filling material. Failure to find and fill a canal contributes toward the failure of endodontic therapy .The root canal anatomy of mandibular first molars is complex. Studies of the morphologic structure of root canal systems hav...
متن کاملObstetrical Complications and Outcome in Two Families with Hereditary Angioedema due to Mutation in the F12 Gene
Backgroud. Hereditary angioedema (HAE) is characterized by recurrent swelling of the skin, the abdomen (causing severe acute pain), and the airways. A recently discovered type caused by mutations in the factor XII gene (designated as HAE type III) occurs mainly in women. Estrogens may play an important role, but few obstetrical complications have been reported. Case. We report the symptoms and ...
متن کاملreport on the first survey of iranian patients with hereditary angioedema
background: hereditary angioedema (hae) is a rare autosomal dominant primary immunodeficiency with complement system defect characterized by recurrent episodes of angioedema involving the skin or mucosa of the upper respiratory and gastrointestinal tracts. objective: to characterize the clinical and laboratory data of hereditary angioedema in iran. methods: patients with probable diagnosis of a...
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ژورنال
عنوان ژورنال: Clinical Medicine
سال: 2016
ISSN: 1470-2118,1473-4893
DOI: 10.7861/clinmedicine.16-2-206