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S Afr Med J ; 50(5): 139-40, 1976 Jan 31.
Artigo em Inglês | MEDLINE | ID: mdl-1251291

RESUMO

A young White girl was found to have no detectable complement C3 or C1q. She suffered repeated attacks of pneumococcal meningitis and pneumococcal pneumonia. Her parents, and some of her siblings, had half the normal level of C3; other siblings were normal. She also had decreased IgG levels and increased IgM concentrations. These findings are correlated with a dysmorphic state of the germinal centres of the peripheral lymphoid tissues, seen after death.


Assuntos
Complemento C3/deficiência , Proteínas do Sistema Complemento/deficiência , Meningite Pneumocócica/genética , Criança , Pré-Escolar , Disgamaglobulinemia/complicações , Feminino , Genes , Humanos , Imunoglobulina G , Lactente , Masculino
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