Diagnosis and identification of hereditary angioedema / 国际药学研究杂志
Journal of International Pharmaceutical Research
; (6): 190-193, 2017.
Article
em Zh
| WPRIM
| ID: wpr-845420
Biblioteca responsável:
WPRO
ABSTRACT
Agioedema, as a clinical symptom, is often combined with wheals and diagnosed as urticaria. As to angioedema without wheals, it is considered an independent disease. According to the causes, angioedema is divided into 2 types: hereditary angioedema and acquired angioedema. As a rare disease, hereditary angioedema is often misdiagnosed and mistreated, mistreated, although it is severe and life-threatening sometimes. It is therefore necessary to introduce how to identify and treat hereditary angioededa patients.
Texto completo:
1
Índice:
WPRIM
Tipo de estudo:
Diagnostic_studies
Idioma:
Zh
Revista:
Journal of International Pharmaceutical Research
Ano de publicação:
2017
Tipo de documento:
Article