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1.
J Pediatr ; 148(3): 404-6, 2006 Mar.
Article in English | MEDLINE | ID: mdl-16615979

ABSTRACT

HyperIgM syndrome is a heterogenous immunodeficiency characterized by impaired class-switch recombination due to different molecular abnormalities. We report on two female patients affected by a novel syndrome associating HIGM, growth and pubertal disturbances, and severe lymphoid hyperplasia with eventual development into lymphomas, suggesting a DNA repair defect.


Subject(s)
Growth Disorders/genetics , Hypergammaglobulinemia/genetics , Immunoglobulin M/blood , Lymphoma, B-Cell/genetics , Puberty, Delayed/genetics , Adolescent , Child , Female , Humans , Lymphatic Diseases/genetics
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