Clinics (Sao Paulo, Brazil) · 2018
Brazilian Guidelines for Hereditary Angioedema Management - 2017 Update Part 1: Definition, Classification and Diagnosis.
СтатьяКлинические рекомендацииНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Giavina-Bianchi Pedro, Arruda Luisa Karla, Aun Marcelo V, Campos Regis A, Chong-Neto Herberto J, Constantino-Silva Rosemeire N, Fernandes Fátima R, Ferraro Maria F, Ferriani Mariana P L, França Alfeu T, Fusaro Gustavo, Garcia Juliana F B, Komninakis Shirley, Maia Luana S M, Mansour Eli, Moreno Adriana S, Motta Antonio A, Pesquero João B, Portilho Nathalia, Rosário Nelson A, Serpa Faradiba S, Solé Dirceu, Takejima Priscila, Toledo Eliana, Valle Solange O.R, Veronez Camila L, Grumach Anete S
Аннотация
Hereditary angioedema is an autosomal dominant disease characterized by recurrent angioedema attacks with the involvement of multiple organs. The disease is unknown to many health professionals and is therefore underdiagnosed. Patients who are not adequately diagnosed and treated have an estimated mortality rate ranging from 25% to 40% due to asphyxiation by laryngeal angioedema. Intestinal angioedema is another important and incapacitating presentation that may be the main or only manifestation during an attack. In this article, a group of experts from the "Associação Brasileira de Alergia e Imunologia (ASBAI)" and the "Grupo de Estudos Brasileiro em Angioedema Hereditário (GEBRAEH)" has updated the Brazilian guidelines for the diagnosis and treatment of hereditary angioedema.