SciELO - Scientific Electronic Library Online

 
vol.40 issue2Association between a combined oral contraceptive and the erythema nodosum: a case reportSecondary Syphilis: decompensation factor of underlying liver disease? A clinical case author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

Related links

  • Have no similar articlesSimilars in SciELO

Share


Revista Portuguesa de Medicina Geral e Familiar

Print version ISSN 2182-5173

Abstract

SANTOS, Filipa Rodrigues dos; FALCAO, Inês  and  CUNHA, Leonor. Hereditary angioedema with normal C1-inhibitor levels: a rare case report. Rev Port Med Geral Fam [online]. 2024, vol.40, n.2, pp.170-172.  Epub Apr 30, 2024. ISSN 2182-5173.  https://doi.org/10.32385/rpmgf.v40i2.13745.

Hereditary angioedema (HAE) is a rare, hereditary disease and its manifestations may be life-threatening. It differs from histaminergic angioedema since it shows different underlying mechanisms and, therefore, does not respond to antihistamine or adrenaline treatment. The authors present a case of hereditary angioedema to highlight the importance of prompt referral to the allergy and clinical immunology for further evaluation and correct diagnosis in case of suspicion of this entity.

Keywords : Hereditary angioedema; Normal C1-inhibitor; FXII gene.

        · abstract in Portuguese     · text in English     · English ( pdf )