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3.
An Esp Pediatr ; 30(6): 499-502, 1989 Jun.
Artigo em Espanhol | MEDLINE | ID: mdl-2679278

RESUMO

We have studied a girl seven and a half years old with a renal disease manifested by proteinuria and nephrotic syndrome combined with initial macroscopic hematuria normal blood pressure and persistent depression of the complement C3 levels with the complement activating gamma globulin (C3 Nef) present in serum. The anatomopathological study showed findings of membranoproliferative glomerulonephritis type II with intramembranous deposit (dense deposit disease). An unusual association with partial lipodystrophy was present in this case. A follow-up of five years, and a few considerations about etiopathogenic theories were presented.


Assuntos
Glomerulonefrite Membranoproliferativa/complicações , Lipodistrofia/complicações , Criança , Complemento C3/análise , Fator Nefrítico do Complemento 3/análise , Feminino , Humanos
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