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Published in 2024 at "Orphanet Journal of Rare Diseases"
DOI: 10.1186/s13023-024-03302-x
Abstract: Background Hereditary Angioedema (HAE) due to C1-inhibitor deficiency (C1INH) is a rare condition, clinically characterised by recurrent swelling. The unpredictability of attacks affects the patients’ quality of life (QoL). HAE patients and their families have…
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Keywords:
human centred;
angioedema;
innovative approach;
centred innovative ... See more keywords