Brazilian guidelines for the diagnosis and treatment of hereditary angioedema
Hereditary angioedema is an autosomal dominant disease characterized by edema attacks with multiple organ involvement. It is caused by a quantitative or functional deficiency of the C1 inhibitor, which is a member of the serine protease inhibitor family. Hereditary angioedema is unknown to many heal...
Main Authors: | , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Faculdade de Medicina / USP
2011-01-01
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Series: | Clinics |
Subjects: | |
Online Access: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1807-59322011000900021 |