The physician and hereditary angioedema friend or foe: 62-year diagnostic delay and iatrogenic procedures
Abstract 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 ha...
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| Principais autores: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMC
2018-10-01
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| coleção: | Allergy, Asthma & Clinical Immunology |
| Assuntos: | |
| Acesso em linha: | http://link.springer.com/article/10.1186/s13223-018-0275-4 |
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