Hereditary angioneurotic oedema: a neglected diagnosis.
نویسندگان
چکیده
A case of hereditary angioneurotic oedema, which was only diagnosed after presentation to several hospital departments, is reported. It was then discovered that the mother of the patient had the same condition but that, unusually, it appeared to have been in remission for more than 20 years. This disease, due to C1 esterase inhibitor deficiency, is potentially fatal but easily treatable. The diagnosis is often missed.
منابع مشابه
Therapy in hereditary angioneurotic oedema.
Gwynn, C. M. (1974). Archives of Disease in Childhood, 49, 636. Therapy in hereditary angioneurotic oedema. Two branches of a family suffering from hereditary angioneurotic oedema underwent trials of therapy of E-amino caproic-acid (EACA) to ascertain the optimum dosage required to alleviate symptoms without giving rise to unpleasant side effects. It was found that children under 11 years toler...
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ورودعنوان ژورنال:
- Journal of clinical pathology
دوره 40 5 شماره
صفحات -
تاریخ انتشار 1987