A case of hereditary angioneurotic oedema, successfully treated with epsilon-aminocaproic acid. Studies on C'1 esterase inhibitor, C'1 activation, plasminogen level and histamine metabolism.
- 1 September 1968
- journal article
- Vol. 3 (7) , 733-45
Abstract
A patient with clinical and laboratory findings characteristic of hereditary angioneurotic oedema was investigated. The patient was observed for a period of 5 weeks, during which he had four attacks. ε-Aminocaproic acid (EACA) was then given continuously for 5 months, during which time the patient had no attacks. Attacks reappeared on withdrawal of EACA. Trans-4-(aminomethyl) cyclohexane carboxylic acid (AMCA®) was found to be equally effective in later therapeutic trials.This publication has 33 references indexed in Scilit:
- EFFECT OF TRYPSIN ON COMPLEMENT COMPONENTS IN NORMAL HUMAN SERUMActa Pathologica Microbiologica Scandinavica, 2009
- Hereditary Periodic OedemaActa Medica Scandinavica, 2009
- C'1-Esterase und C'1-Esterase-Inhibitor im Serum von Kranken mit hereditärem genuinem Quincke-ÖdemKlinische Wochenschrift, 1967
- A Method for Semiquantitative Determination of 1-Methyl-4-Imidazoleacetic Acid in Human UrineScandinavian Journal of Clinical and Laboratory Investigation, 1965
- THE MACROMOLECULAR NATURE OF THE FIRST COMPONENT OF HUMAN COMPLEMENTThe Journal of Experimental Medicine, 1964
- CHROMATOGRAPHIC RESOLUTION OF THE FIRST COMPONENT OF HUMAN COMPLEMENT INTO THREE ACTIVITIESThe Journal of Experimental Medicine, 1963
- Hereditary angioneurotic edema: II. Deficiency of inhibitor for serum globulin permeability factor and/or plasma kallikreinJournal of Allergy, 1962
- Hereditary angioneurotic edema: I. Case reports and review of the literatureJournal of Allergy, 1962
- STUDIES ON THE ACTIVATION OF A PROESTERASE ASSOCIATED WITH PARTIALLY PURIFIED FIRST COMPONENT OF HUMAN COMPLEMENTThe Journal of Experimental Medicine, 1958
- THE PROPERDIN SYSTEM AND IMMUNITYThe Journal of Experimental Medicine, 1956