Hereditary Angioedema: Diagnosis, Clinical Implications, and Pathophysiology

Hereditary angioedema (HAE) is an autosomal dominant disorder caused by a mutation in the C1 esterase inhibitor gene. HAE affects 1/50,000 people worldwide. Three main types of HAE exist: type I, type II, and type III. Type I is characterized by a deficiency in C1-INH. C1-INH is important in the coa...

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Detalles Bibliográficos
Autores principales: Sinnathamby, Evan S., Issa, Peter P., Roberts, Logan, Norwood, Haley, Malone, Kevin, Vemulapalli, Harshitha, Ahmadzadeh, Shahab, Cornett, Elyse M., Shekoohi, Sahar, Kaye, Alan D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9988798/
https://www.ncbi.nlm.nih.gov/pubmed/36609679
http://dx.doi.org/10.1007/s12325-022-02401-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9988798/
https://www.ncbi.nlm.nih.gov/pubmed/36609679
http://dx.doi.org/10.1007/s12325-022-02401-0

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