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

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

Abstract 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 Da...

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Bibliographic Details
Main Authors: Irina Guryanova, Chiara Suffritti, Debora Parolin, Andrea Zanichelli, Nastassia Ishchanka, Ekaterina Polyakova, Mikhail Belevtsev, Francesca Perego, Marco Cicardi, Yulia Zharankova, Natalya Konoplya, Sonia Caccia, Antonio Gidaro
Format: Article
Language:English
Published: BMC 2021-04-01
Series:Clinical and Molecular Allergy
Subjects:
Belarus
C1 inhibitor
Hereditary angioedema (HAE)
Rare disease
SERPING1 variants
Online Access:https://doi.org/10.1186/s12948-021-00141-0

Internet

https://doi.org/10.1186/s12948-021-00141-0

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