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The physician and hereditary angioedema friend or foe: 62-year diagnostic delay and iatrogenic procedures

20:00 EDT 24 Oct 2018 | Allergy Asthma and Clinical Immunology

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 dise...

Original Article: The physician and hereditary angioedema friend or foe: 62-year diagnostic delay and iatrogenic procedures

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