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Annals of Saudi Medicine. 2010; 30 (3): 239-242
in English | IMEMR | ID: emr-98769

ABSTRACT

Severe combined immunodeficiency [SCID] is a primary immunodeficiency disorder with heterogenous genetic etiologies. We describe a typical case in a 9-year-old boy that was masked by a clinically functional maternal T cell engraftment leading to late presentation with Pneumocystis jiroveci pneumonia and cytomegalovirus infection, probably following exhaustion of maternally engrafted cells. Based on immunological findings, he had a T- B+SCID phenotype.This report suggests that in rare cases, engrafted maternal T cell might persist for long time leading to partial constitution of immune function and delayed clinical presentation of SCID


Subject(s)
Humans , Male , Child , Severe Combined Immunodeficiency/physiopathology , Pneumocystis carinii , Pneumocystis Infections/diagnosis , Cytomegalovirus Infections
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