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Newborn Screening for Pompe Disease.
Bodamer, Olaf A; Scott, C Ronald; Giugliani, Roberto.
Afiliación
  • Bodamer OA; Division of Genetics and Genomics, Boston Children's Hospital, Boston, Massachusetts; olaf.bodamer@childrens.harvard.edu.
  • Scott CR; Division of Molecular Medicine, Department of Pediatrics, University of Washington, Seattle, Washington; and.
  • Giugliani R; Medical Genetics Service, Hospital de Clinicas de Porto Alegre (HCPA) and Department of Genetics, Federal University of Rio Grande do Sul (UFRGS), Porto Alegre, Brazil.
Pediatrics ; 140(Suppl 1): S4-S13, 2017 Jul.
Article en En | MEDLINE | ID: mdl-29162673
ABSTRACT
Started in 1963 by Robert Guthrie, newborn screening (NBS) is considered to be one of the great public health achievements. Its original goal was to screen newborns for conditions that could benefit from presymptomatic treatment, thereby reducing associated morbidity and mortality. With advances in technology, the number of disorders included in NBS programs increased. Pompe disease is a good candidate for NBS. Because decisions regarding which diseases should be included in NBS panels are made regionally and locally, programs and efforts for NBS for Pompe disease have been inconsistent both in the United States and globally. In this article, published in the "Newborn Screening, Diagnosis, and Treatment for Pompe Disease" guidance supplement, the Pompe Disease Newborn Screening Working Group, an international group of experts in both NBS and Pompe disease, review the methods used for NBS for Pompe disease and summarize results of current and ongoing NBS programs in the United States and other countries. Challenges and potential drawbacks associated with NBS also are discussed.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 2_ODS3 / 6_ODS3_enfermedades_notrasmisibles / 7_ODS3_muertes_prevenibles_nacidos_ninos Problema de salud: 2_muertes_prevenibles / 6_endocrine_disorders / 7_neonatal_care_health / 7_nutrition Asunto principal: Enfermedad del Almacenamiento de Glucógeno Tipo II / Tamizaje Neonatal Tipo de estudio: Diagnostic_studies / Guideline / Prognostic_studies / Screening_studies Límite: Humans / Newborn Idioma: En Revista: Pediatrics Año: 2017 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 2_ODS3 / 6_ODS3_enfermedades_notrasmisibles / 7_ODS3_muertes_prevenibles_nacidos_ninos Problema de salud: 2_muertes_prevenibles / 6_endocrine_disorders / 7_neonatal_care_health / 7_nutrition Asunto principal: Enfermedad del Almacenamiento de Glucógeno Tipo II / Tamizaje Neonatal Tipo de estudio: Diagnostic_studies / Guideline / Prognostic_studies / Screening_studies Límite: Humans / Newborn Idioma: En Revista: Pediatrics Año: 2017 Tipo del documento: Article
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