Hereditary angioedema due to C1 inhibitor deficiency in Belarus: epidemiology, access to diagnosis and seven novel mutations in SERPING1 gene

BACKGROUND: Hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE) is a rare disease. Few states in developing countries have an adequate management of HAE, but none of them belongs to the former USSR area. This study analyses data from C1-INH-HAE patients from Belarus. METHODS: Data abou...

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Detalles Bibliográficos
Autores principales: Guryanova, Irina, Suffritti, Chiara, Parolin, Debora, Zanichelli, Andrea, Ishchanka, Nastassia, Polyakova, Ekaterina, Belevtsev, Mikhail, Perego, Francesca, Cicardi, Marco, Zharankova, Yulia, Konoplya, Natalya, Caccia, Sonia, Gidaro, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8028818/
https://www.ncbi.nlm.nih.gov/pubmed/33827715
http://dx.doi.org/10.1186/s12948-021-00141-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8028818/
https://www.ncbi.nlm.nih.gov/pubmed/33827715
http://dx.doi.org/10.1186/s12948-021-00141-0

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