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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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| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
BioMed Central
2010
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| Accès en ligne: | 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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