Posttransplant outcome of atypical haemolytic uraemic syndrome in a patient with thrombomodulin mutation: a case without recurrence

Atypical haemolytic uraemic syndrome (aHUS) is a rare disease characterized by thrombocytopenia, microangiopathic haemolytic anaemia and renal impairment. Mutations in genes encoding inhibitors of the alternative pathway of the complement system are involved in ∼50% of the cases. Thrombomodulin (THB...

Descripción completa

Detalles Bibliográficos
Autores principales: Caroti, Leonardo, Di Maria, Lorenzo, Carta, Paolo, Moscarelli, Luciano, Cirami, Calogero, Minetti, Enrico Eugenio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Contents
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4440472/
https://www.ncbi.nlm.nih.gov/pubmed/26034596
http://dx.doi.org/10.1093/ckj/sfv025

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4440472/
https://www.ncbi.nlm.nih.gov/pubmed/26034596
http://dx.doi.org/10.1093/ckj/sfv025

Ejemplares similares