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Pediatric hereditary angioedema due to C1-inhibitor deficiency

Hereditary angioedema (HAE) resulting from the deficiency of the C1 inhibitor (C1-INH) is a rare, life-threatening disorder. It is characterized by attacks of angioedema involving the skin and/or the mucosa of the upper airways, as well as the intestinal mucosa. In approximately 50 per cent of cases...

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Bibliografske podrobnosti
Glavni avtor: Farkas, Henriette
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2010
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC2920237/
https://ncbi.nlm.nih.gov/pubmed/20667121
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1710-1492-6-18
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