Please use this identifier to cite or link to this item: https://observatorio.fm.usp.br/handle/OPI/38505
Title: Lymphoproliferative disorder with polyautoimmunity and hypogammaglobulinemia: An unusual presentation of 22q11.2 deletion syndrome
Authors: SOARES, Diogo C.DANTAS, Anelisa G.MATTA, Marina C.PASTORINO, Antonio C.MELARAGNO, Maria IsabelKULIKOWSKI, LeslieMONTENEGRO, MariliaKIM, Chong A.CARNEIRO-SAMPAIO, MagdaTORRES, Leuridan C.
Citation: CLINICAL IMMUNOLOGY, v.220, article ID 108590, 3p, 2020
Abstract: 22q11.2 deletion syndrome (22q11.2DS) has a heterogeneous presentation that includes multiple congenital anomalies and immunodeficiency, one of the most striking features. Usually, it is characterized by T cell lymphopenia, B cell dysfunction and autoimmunity. Here, we describe an unusual case of 22q11.2DS in a patient with lymphoproliferative disorder, polyautoimmunity and hypogammaglobulinemia.
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Artigos e Materiais de Revistas Científicas - FM/MPE
Departamento de Pediatria - FM/MPE

Artigos e Materiais de Revistas Científicas - HC/ICr
Instituto da Criança - HC/ICr

Artigos e Materiais de Revistas Científicas - LIM/03
LIM/03 - Laboratório de Medicina Laboratorial

Artigos e Materiais de Revistas Científicas - LIM/36
LIM/36 - Laboratório de Pediatria Clínica

Artigos e Materiais de Revistas Científicas - ODS/03
ODS/03 - Saúde e bem-estar


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