摘要Hereditary angioedema(HAE)is a rare,autosomal dominant inherited disorder with an incidence of approximately 1 in 50,000.Among its various tapes,HAE with normal C1 inhibitor levels(HAE-nC1-INH)is exceptionally rare.[1]HAE symptoms include recurrent episodes of skin and mucosal edema that can occur anywhere in the body.[1-4]Laryngeal edema is life-threatening,as it can lead to airway obstruction and potentially fatal suffocation.
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