Lymphoproliferative disorder with polyautoimmunity and hypogammaglobulinemia An unusual presentation of 22q11.2 deletion syndrome

Lymphoproliferative disorder with polyautoimmunity and hypogammaglobulinemia : An unusual presentation of 22q11.2 deletion syndrome

Copyright © 2020 Elsevier Inc. All rights reserved.

Bibliographische Detailangaben
Veröffentlicht in:Clinical immunology (Orlando, Fla.). - 1999. - 220(2020) vom: 28. Nov., Seite 108590
1. Verfasser: Soares, Diogo C (VerfasserIn)
Weitere Verfasser: Dantas, Anelisa G, Matta, Marina C, Pastorino, Antonio C, Melaragno, Maria Isabel, Kulikowski, Leslie, Montenegro, Marilia, Kim, Chong A, Carneiro-Sampaio, Magda, Torres, Leuridan C
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2020
Zugriff auf das übergeordnete Werk:Clinical immunology (Orlando, Fla.)
Schlagworte:Case Reports Letter Research Support, Non-U.S. Gov't 22q11.2 deletion syndrome Autoimmunity DiGeorge syndrome Hypogammaglobulinemia Immunodeficiency
Beschreibung
Zusammenfassung:Copyright © 2020 Elsevier Inc. All rights reserved.
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
Beschreibung:Date Completed 14.05.2021
Date Revised 14.05.2021
published: Print-Electronic
Citation Status MEDLINE
ISSN:1521-7035
DOI:10.1016/j.clim.2020.108590