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dc.contributorSistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP
dc.contributor.authorSOARES, Diogo C.
dc.contributor.authorDANTAS, Anelisa G.
dc.contributor.authorMATTA, Marina C.
dc.contributor.authorPASTORINO, Antonio C.
dc.contributor.authorMELARAGNO, Maria Isabel
dc.contributor.authorKULIKOWSKI, Leslie
dc.contributor.authorMONTENEGRO, Marilia
dc.contributor.authorKIM, Chong A.
dc.contributor.authorCARNEIRO-SAMPAIO, Magda
dc.contributor.authorTORRES, Leuridan C.
dc.date.accessioned2020-12-16T14:56:47Z-
dc.date.available2020-12-16T14:56:47Z-
dc.date.issued2020
dc.identifier.citationCLINICAL IMMUNOLOGY, v.220, article ID 108590, 3p, 2020
dc.identifier.issn1521-6616
dc.identifier.urihttps://observatorio.fm.usp.br/handle/OPI/38505-
dc.description.abstract22q11.2 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.eng
dc.description.sponsorshipFAPESPFundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [2014/11572-8, 2014/50489-9]
dc.description.sponsorshipCAPESCAPES [001]
dc.language.isoeng
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCEeng
dc.relation.ispartofClinical Immunology
dc.rightsrestrictedAccesseng
dc.subjectDiGeorge syndromeeng
dc.subject22q11.2 deletion syndromeeng
dc.subjectImmunodeficiencyeng
dc.subjectAutoimmunityeng
dc.subjectHypogammaglobulinemiaeng
dc.subject.otherresponseseng
dc.titleLymphoproliferative disorder with polyautoimmunity and hypogammaglobulinemia: An unusual presentation of 22q11.2 deletion syndromeeng
dc.typearticleeng
dc.rights.holderCopyright ACADEMIC PRESS INC ELSEVIER SCIENCEeng
dc.identifier.doi10.1016/j.clim.2020.108590
dc.identifier.pmid32920211
dc.subject.wosImmunologyeng
dc.type.categorylettereng
dc.type.versionpublishedVersioneng
hcfmusp.author.externalDANTAS, Anelisa G.:Univ Fed Sao Paulo UNIFESP, Div Genet, Dept Morphol & Genet, Sao Paulo, SP, Brazil
hcfmusp.author.externalMATTA, Marina C.:Inst Med Integral Prof Fernando Figueira IMIP, Translat Res Lab, Recife, PE, Brazil
hcfmusp.author.externalMELARAGNO, Maria Isabel:Univ Fed Sao Paulo UNIFESP, Div Genet, Dept Morphol & Genet, Sao Paulo, SP, Brazil
hcfmusp.author.externalTORRES, Leuridan C.:Inst Med Integral Prof Fernando Figueira IMIP, Translat Res Lab, Recife, PE, Brazil
hcfmusp.description.articlenumber108590
hcfmusp.description.volume220
hcfmusp.origemWOS
hcfmusp.origem.idWOS:000582396200009
hcfmusp.origem.id2-s2.0-85091232100
hcfmusp.publisher.citySAN DIEGOeng
hcfmusp.publisher.countryUSAeng
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dc.description.indexMEDLINEeng
dc.identifier.eissn1521-7035
hcfmusp.citation.scopus1-
hcfmusp.scopus.lastupdate2024-03-29-
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ODS/03 - Saúde e bem-estar


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