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Hereditary Angioedema Due to C1-Inhibitor Deficiency in Romania: First National Study, Diagnostic and Treatment Challenges

Gabriella Gabos; Valentin Nadasan; Eniko Mihaly; Daniela Dobru

Volume 17, Issue 3 , September 2020, , Pages 226-235

https://doi.org/10.22034/iji.2020.85416.1709

Abstract
  Background: Hereditary angioedema (HAE) is a rare genetic potentially life-threatening disease characterized by episodic non-pruritic subcutaneous and submucosal edema attacks in different parts of the body. Objective: To assess the status of Romanian HAE patients after the recent introduction of a new ...  Read More