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Asia Pac Allergy ; 13(2): 88-90, 2023 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-37388811

RESUMEN

We report 2 patients who first developed cutaneous manifestations, followed by autoimmune phenomena, infections, and hypogammaglobulinemia. They were initially diagnosed with common variable immunodeficiency; however, the diagnosis was revised to cytotoxic T-lymphocyte antigen 4 haploinsufficiency after genetic and functional testing.

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