Literature DB >> 11132070

Unusual manifestations of hereditary angioedema.

S Neri1, D Ierna, L Sfogliano.   

Abstract

Hereditary angioedema is a hereditary disorder transmitted as an autosomal dominant trait, characterized by reduced plasma concentration of C1 esterase inhibitor (type 1) or the presence of non functional C1 esterase inhibitor (type 2). We describe and discuss the case of a 35-year-old man who presented two unusual clinical manifestations of type 2 hereditary angioedema causing diverse emergency situations: acute abdomen and parasellar oedema.

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Year:  2000        PMID: 11132070     DOI: 10.1097/00063110-200006000-00004

Source DB:  PubMed          Journal:  Eur J Emerg Med        ISSN: 0969-9546            Impact factor:   2.799


  2 in total

Review 1.  Hereditary angioedema in childhood: an approach to management.

Authors:  Didier G Ebo; Marjoke M Verweij; Kathleen J De Knop; Margo M Hagendorens; Chris H Bridts; Luc S De Clerck; Wim J Stevens
Journal:  Paediatr Drugs       Date:  2010-08-01       Impact factor: 3.022

Review 2.  Hereditary angioedema: imaging manifestations and clinical management.

Authors:  Mandip S Gakhal; Gregory V Marcotte
Journal:  Emerg Radiol       Date:  2014-06-01
  2 in total

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