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Pediatr Infect Dis J ; 38(2): 157-160, 2019 02.
Article in English | MEDLINE | ID: mdl-29613974

ABSTRACT

Newborn screening for severe combined immunodeficiency using T-cell receptor excision circles allows prompt diagnosis and initiation of supportive and curative therapy thereby reducing morbidity and mortality. However, profound combined immunodeficiencies with normal numbers of nonfunctional T cells will go undetected. We present a patient with calcium release-activated calcium channel gene (ORAI1) deficiency and normal T-cell receptor excision circle numbers observed after diagnosis at the age of 14 months who suffered from disseminated fatal cytomegalovirus and Pneumocystis jirovecii infection, demonstrating a potential pitfall of the current newborn screening program.


Subject(s)
Cytomegalovirus Infections/diagnosis , Cytomegalovirus/isolation & purification , Diagnostic Tests, Routine/methods , Neonatal Screening/methods , Pneumocystis carinii/isolation & purification , Pneumonia, Pneumocystis/diagnosis , Severe Combined Immunodeficiency/diagnosis , Cytomegalovirus Infections/complications , Cytomegalovirus Infections/pathology , Fatal Outcome , Female , Humans , Infant , Infant, Newborn , Pneumonia, Pneumocystis/complications , Pneumonia, Pneumocystis/pathology , Severe Combined Immunodeficiency/complications , T-Lymphocytes/pathology
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