The physician and hereditary angioedema friend or foe: 62-year diagnostic delay and iatrogenic procedures
Abstract
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 occur if HAE is not considered in the differential diagnosis, the specialists are not aware of the natural history, diagnosis and treatment of HAE, or as a result...
Paper Details
Title
The physician and hereditary angioedema friend or foe: 62-year diagnostic delay and iatrogenic procedures
Published Date
Oct 25, 2018
Volume
14
Issue
1
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