A Case of Type 2 Hereditary Angioedema With SERPING1 Mutation

Hereditary angioedema is a disease of congenital deficiency or functional defect in the C1 esterase inhibitor (C1-INH) consequent to mutation in the SERPING1 gene, which encodes C1-INH. This disease manifests as recurrent, non-pitting, non-pruritic subcutaneous, or submucosal edema as well as an ery...

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Detalles Bibliográficos
Autores principales: Sim, Da Woon, Park, Kyung Hee, Lee, Jae-Hyun, Park, Jung-Won
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Academy of Asthma, Allergy and Clinical Immunology; The Korean Academy of Pediatric Allergy and Respiratory Disease 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5102842/
https://www.ncbi.nlm.nih.gov/pubmed/27826968
http://dx.doi.org/10.4168/aair.2017.9.1.96

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5102842/
https://www.ncbi.nlm.nih.gov/pubmed/27826968
http://dx.doi.org/10.4168/aair.2017.9.1.96

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