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Incidence of severe combined immunodeficiency through newborn screening in a Chinese population.
Chien, Yin-Hsiu; Chiang, Shu-Chuan; Chang, Kai-Ling; Yu, Hsin-Hui; Lee, Wen-I; Tsai, Li-Ping; Hsu, Li-Wen; Hu, Min-Huei; Hwu, Wuh-Liang.
Afiliação
  • Chien YH; Department of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan; Department of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan.
  • Chiang SC; Department of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan.
  • Chang KL; Department of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan.
  • Yu HH; Department of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan.
  • Lee WI; Department of Pediatrics, Chang Gung Memorial Hospital and Children's Hospital, Chang Gung University College of Medicine, Taoyuan, Taiwan.
  • Tsai LP; Department of Pediatrics, Buddhist Tzu Chi General Hospital, Taipei Branch, New Taipei City, Taiwan.
  • Hsu LW; Department of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan.
  • Hu MH; Department of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan.
  • Hwu WL; Department of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan; Department of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan. Electronic address: hwuwlntu@ntu.edu.tw.
J Formos Med Assoc ; 114(1): 12-6, 2015 Jan.
Article em En | MEDLINE | ID: mdl-25618583
BACKGROUND/PURPOSE: In order to know the true incidence of severe combined immunodeficiency (SCID) in a Chinese population, we conducted and implemented SCID newborn screening in Taiwan. METHODS: Between May 1, 2010 and December 31, 2011, the National Taiwan University Hospital Newborn Screening Center screened all newborns for T-cell lymphopenia by measuring the copy number of T-cell receptor excision circles (TRECs) and RNase P. Newborns with low TREC values were subjected to complete blood cell counts and flow cytometry. RESULTS: A total of 106,391 newborns were screened using the TREC assay over a period of 19 months. Five newborns were immediately referred for confirmatory tests, including two SCID patients and two patients with persistent T-cell lymphopenia; a third SCID patient was found 2 months after the study period. All three SCID cases received stem cell transplantation at the age of 2-5 months. We also identified five cases of 22q11.2 microdeletion syndrome. During this period, two SCID patients from among the unscreened newborns were reported, and they died at ages 3 months and 4 months, respectively. CONCLUSION: Newborn screening to measure the number of TREC copies successfully identifies newborns with T-cell lymphopenia, 22q11.2 microdeletion syndrome, and other high-risk conditions. Taken together, the incidence of T-cell lymphopenia in apparently healthy newborns is more than 1 in 11,821, and further attention to their immune functions is warranted.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Triagem Neonatal / Imunodeficiência Combinada Severa / Linfopenia Tipo de estudo: Diagnostic_studies / Incidence_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Female / Humans / Infant / Male / Newborn País/Região como assunto: Asia Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Triagem Neonatal / Imunodeficiência Combinada Severa / Linfopenia Tipo de estudo: Diagnostic_studies / Incidence_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Female / Humans / Infant / Male / Newborn País/Região como assunto: Asia Idioma: En Ano de publicação: 2015 Tipo de documento: Article