Abdominal and pelvic imaging in the diagnosis of acute abdominal attacks in patients with hereditary angioedema due to C1-inhibitor deficiency

INTRODUCTION: Hereditary angioedema (HAE) is a rare inherited autosomal dominant disease caused by deficiency or dysfunction of C1 inhibitor (C1INH). Clinical symptoms include recurrent subcutaneous and submucosal angioedema of the internal organs. Abdominal attacks affect more than 90% of patients,...

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Detalles Bibliográficos
Autores principales: Obtułowicz, Piotr, Stobiecki, Marcin, Dyga, Wojciech, Juchacz, Aldona, Popiela, Tadeusz, Obtułowicz, Krystyna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2021
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9454366/
https://www.ncbi.nlm.nih.gov/pubmed/36090726
http://dx.doi.org/10.5114/ada.2021.108438

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9454366/
https://www.ncbi.nlm.nih.gov/pubmed/36090726
http://dx.doi.org/10.5114/ada.2021.108438

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