Diagnostic and therapeutic management of hereditary angioedema due to C1-inhibitor deficiency: the Italian experience
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Purpose of review: Hereditary angioedema (HAE) due to C1-inhibitor (C1-INH) deficiency (C1-INH-HAE) is a rare disease, with a reported prevalence of about 1 : 50 000. C1-INH-HAE causes disabling symptoms, which may be life-threat... ...
