Objective: To understand the patient’s journey with HAE from symptom initiation to diagnosis, treatment allocation, follow-up, and impact of disease on their quality life in Mexico. Methods: A survey was administered patients HAE. Participants completed a questionnaire covering five domains: patient journey; effects productivity, school performance daily activities; life; anxiety depression. Re...

Hereditary angioedema (HAE) is a rare inherited disease that is often difficult to diagnose. We report a case of a 9-year-old boy with a spontaneous mutation causing HAE, diagnosed after a life-threatening episode of angioedema of the head and upper respiratory tract after a 5-year history of recurrent skin swellings and abdominal pain leading to several hospital admissions. The aim of this rep...