A Germany-wide survey study on the patient journey of patients with hereditary angioedema | Orphanet Journal of Rare Diseases | Full Text

A Germany-wide survey study on the patient journey of patients with hereditary angioedema | Orphanet Journal of Rare Diseases | Full Text

A Germany-wide survey study on the patient journey of patients with hereditary angioedema

Hereditary angioedema (HAE) is a rare genetic disease and characterized by clinical features such as paroxysmal, recurrent angioedema of the skin, the gastrointestinal tract, and the upper airways. Swelling of...

Authors:Markus Magerl, Holger Gothe, Simon Krupka, Anja Lachmann and Christoph Ohlmeier

Citation:Orphanet Journal of Rare Diseases 2020 15:221

Content type:Research

 

Published on: 26 August 2020

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