Hereditary Angioedema: a Challenging Diagnosis for the Gastroenterologist
Hereditary angioedema (HAE) caused by a deficiency of C1 esterase inhibitor enzyme (C1-INH) is a very rare, autosomal dominantly inherited genetic disorder, characterized by recurrent peripheral angioedema, painful abdominal attacks and episodes of laryngeal edema. Abdominal attacks are frequent sym...
Main Authors: | Gábos Gabriella, Moldovan Dumitru, Dobru Daniela |
---|---|
Format: | Article |
Language: | English |
Published: |
Sciendo
2016-12-01
|
Series: | Journal of Interdisciplinary Medicine |
Subjects: | |
Online Access: | https://doi.org/10.1515/jim-2016-0072 |
Similar Items
-
Diagnosis and screening of patients with hereditary angioedema in primary care
by: Henao MP, et al.
Published: (2016-05-01) -
Angioedema hereditário: considerações sobre terapia Therapeutic approach of hereditary angioedema
by: Kélem de Nardi Chagas, et al.
Published: (2004-09-01) -
Increased fibrinolysis-induced bradykinin formation in hereditary angioedema confirmed using stored plasma and biotechnological inhibitors
by: François Marceau, et al.
Published: (2019-05-01) -
Mutational spectrum and genotype-phenotype relationships in a cohort of Romanian hereditary angioedema patients caused by C1 inhibitor deficiency
by: Gábos Gabriella, et al.
Published: (2019-07-01) -
A case of hereditary angioedema (type III) in which mandibular wisdom tooth extraction was performed under intravenous sedation management without prophylactic administration of C1–INH
by: Masahiro Morimoto, et al.
Published: (2020-06-01)