Risk of Atypical HUS Among Family Members of Patients Carrying Complement Regulatory Gene Abnormality

INTRODUCTION: Atypical hemolytic uremic syndrome (aHUS) is mainly due to complement regulatory gene abnormalities with a dominant pattern but incomplete penetrance. Thus, healthy carriers can be identified in any family of aHUS patients, but it is unpredictable if they will eventually develop aHUS....

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Detalles Bibliográficos
Autores principales: Ardissino, Gianluigi, Longhi, Selena, Porcaro, Luigi, Pintarelli, Giulia, Strumbo, Bice, Capone, Valentina, Cresseri, Donata, Loffredo, Giulia, Tel, Francesca, Salardi, Stefania, Sgarbanti, Martina, Martelli, Laura, Rodrigues, Evangeline Millicent, Borsa-Ghiringhelli, Nicolò, Montini, Giovanni, Seia, Manuela, Cugno, Massimo, Carfagna, Fabio, Consonni, Dario, Tedeschi, Silvana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Clinical Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8207326/
https://www.ncbi.nlm.nih.gov/pubmed/34169201
http://dx.doi.org/10.1016/j.ekir.2021.03.885

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8207326/
https://www.ncbi.nlm.nih.gov/pubmed/34169201
http://dx.doi.org/10.1016/j.ekir.2021.03.885

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