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The physician and hereditary angioedema friend or foe: 62-year diagnostic delay and iatrogenic procedures
BACKGROUND: Hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE) is a rare autosomal dominant disease characterized by episodes of acute subcutaneous swelling, and/or recurrent severe abdominal pain. The disease is potentially fatal if the upper-airway is involved. Iatrogenic harm can o...
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| Publicado no: | Allergy Asthma Clin Immunol |
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| Principais autores: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6201585/ https://ncbi.nlm.nih.gov/pubmed/30386388 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13223-018-0275-4 |
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