Literature DB >> 3584501

Hereditary angioneurotic oedema: a neglected diagnosis.

G E Morris, B M Slavin, N L Browse.   

Abstract

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.

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Year:  1987        PMID: 3584501      PMCID: PMC1141015          DOI: 10.1136/jcp.40.5.516

Source DB:  PubMed          Journal:  J Clin Pathol        ISSN: 0021-9746            Impact factor:   3.411


  6 in total

1.  Hereditary angioedema: the clinical syndrome and its management.

Authors:  M M Frank; J A Gelfand; J P Atkinson
Journal:  Ann Intern Med       Date:  1976-05       Impact factor: 25.391

2.  Hereditary angioneurotic edema. II. Deficiency of inhibitor for serum globulin permeability factor and/or plasma kallikrein.

Authors:  N S LANDERMAN; M E WEBSTER; E L BECKER; H E RATCLIFFE
Journal:  J Allergy       Date:  1962 Jul-Aug

3.  Hereditary angioneurotic edema. I. Case reports and review of the literature.

Authors:  N S LANDERMAN
Journal:  J Allergy       Date:  1962 Jul-Aug

Review 4.  Hereditary angioedema.

Authors:  C M Brickman; S W Hosea
Journal:  Int J Dermatol       Date:  1983-04       Impact factor: 2.736

5.  Management of hereditary angio-oedema with low-dose danazol.

Authors:  J T MacFarlane; D Davies
Journal:  Br Med J (Clin Res Ed)       Date:  1981-04-18

6.  Hereditary angioedema: an appraisal of 104 cases.

Authors:  M Cicardi; L Bergamaschini; B Marasini; G Boccassini; A Tucci; A Agostoni
Journal:  Am J Med Sci       Date:  1982 Jul-Aug       Impact factor: 2.378

  6 in total

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