A complementary component to atypical haemolytic uraemic syndrome.
BMJ Case Rep
; 20132013 Jun 18.
Article
em En
| MEDLINE
| ID: mdl-23780777
ABSTRACT
We describe a case of a 22-year-old man who presented with clinical features of atypical haemolytic uraemic syndrome and in whom genetic analysis of complement regulatory proteins demonstrated a CD46 mutation. He was treated with plasma exchange, intermittent haemodialysis and blood transfusions. At 6-month follow-up his haematological parameters and renal function showed complete resolution, and he experienced no further disease recurrence in the subsequent year.
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Proteínas do Sistema Complemento
/
Síndrome Hemolítico-Urêmica
Idioma:
En
Ano de publicação:
2013
Tipo de documento:
Article