Hereditary angioedema type 2 presented as an orbital complication of acute rhinosinusitis.

Abstract

Hereditary angioedema is an autosomal dominant and life-threatening disorder characterized by recurrent episodes of non-pitting edema affecting the skin, respiratory system and digestive tracts and caused by a congenital deficiency or function defect of the C1 esterase inhibitor. Preseptal cellulitis is defined as an infection of the tissues of the anterior… (More)
DOI: 10.1016/j.ijporl.2015.12.030

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