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Severe T-cell lymphopenia in a patient with microduplication 22q11.2 identified by newborn screening.
Soomann, Maarja; Prader, Seraina; Lorenzini, Tiziana; Soulard, Clara; Sayasith, Khampoun; Haddad, Elie; Pachlopnik Schmid, Jana.
Afiliação
  • Soomann M; Division of Immunology and the Children's Research Center, University Children's, Hospital Zurich, University of Zurich, Zurich, Switzerland. Electronic address: Maarja.Soomann@kispi.uzh.ch.
  • Prader S; Division of Immunology and the Children's Research Center, University Children's, Hospital Zurich, University of Zurich, Zurich, Switzerland.
  • Lorenzini T; Division of Immunology and the Children's Research Center, University Children's, Hospital Zurich, University of Zurich, Zurich, Switzerland.
  • Soulard C; Department of Pediatrics, University of Montreal, Montreal, Quebec, Canada; Department of Microbiology, Immunology and Infectious Diseases, University of Montreal, Montreal, Quebec, Canada.
  • Sayasith K; Department of Pediatrics, University of Montreal, Montreal, Quebec, Canada.
  • Haddad E; Department of Pediatrics, University of Montreal, Montreal, Quebec, Canada; Department of Microbiology, Immunology and Infectious Diseases, University of Montreal, Montreal, Quebec, Canada; Research Center, Centre hospitalier universitaire (CHU) Sainte-Justine (CHU), Montreal, Quebec, Canada.
  • Pachlopnik Schmid J; Division of Immunology and the Children's Research Center, University Children's, Hospital Zurich, University of Zurich, Zurich, Switzerland.
J Allergy Clin Immunol Pract ; 12(8): 2199-2200.e1, 2024 Aug.
Article em En | MEDLINE | ID: mdl-38729303
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 22 / Linfócitos T / Triagem Neonatal / Síndrome de DiGeorge / Linfopenia Limite: Female / Humans / Male / Newborn Idioma: En Revista: J Allergy Clin Immunol Pract Ano de publicação: 2024 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 22 / Linfócitos T / Triagem Neonatal / Síndrome de DiGeorge / Linfopenia Limite: Female / Humans / Male / Newborn Idioma: En Revista: J Allergy Clin Immunol Pract Ano de publicação: 2024 Tipo de documento: Article