Your browser doesn't support javascript.
loading
Newborn screening for X-linked adrenoleukodystrophy: evidence summary and advisory committee recommendation.
Kemper, Alex R; Brosco, Jeffrey; Comeau, Anne Marie; Green, Nancy S; Grosse, Scott D; Jones, Elizabeth; Kwon, Jennifer M; Lam, Wendy K K; Ojodu, Jelili; Prosser, Lisa A; Tanksley, Susan.
Afiliación
  • Kemper AR; Duke Clinical Research Institute, Duke University, Durham, North Carolina, USA.
  • Brosco J; Department of Pediatrics, University of Miami, Coral Gables, Florida, USA.
  • Comeau AM; Department of Pediatrics, University of Massachusetts Medical School, Jamaica Plain, Massachusetts, USA.
  • Green NS; Department of Pediatrics, Columbia University Medical Center, New York, New York, USA.
  • Grosse SD; National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
  • Jones E; Association of Public Health Laboratories, Silver Spring, Maryland, USA.
  • Kwon JM; Department of Neurology, University of Rochester Medical Center, Rochester, New York, USA.
  • Lam WK; Duke Clinical Research Institute, Duke University, Durham, North Carolina, USA.
  • Ojodu J; Association of Public Health Laboratories, Silver Spring, Maryland, USA.
  • Prosser LA; Child Health Evaluation and Research Unit, Department of Pediatrics, University of Michigan, Ann Arbor, Michigan, USA.
  • Tanksley S; Texas Department of State Health Services, Austin, Texas, USA.
Genet Med ; 19(1): 121-126, 2017 01.
Article en En | MEDLINE | ID: mdl-27337030
ABSTRACT
The secretary of the US Department of Health and Human Services in February 2016 recommended that X-linked adrenoleukodystrophy (X-ALD) be added to the recommended uniform screening panel for state newborn screening programs. This decision was informed by data presented on the accuracy of screening from New York, the only state that currently offers X-ALD newborn screening, and published and unpublished data showing health benefits of earlier treatment (hematopoietic stem cell transplantation and adrenal hormone replacement therapy) for the childhood cerebral form of X-ALD. X-ALD newborn screening also identifies individuals with later-onset disease, but poor genotype-phenotype correlation makes predicting health outcomes difficult and might increase the risk of unnecessary treatment. Few data are available regarding the harms of screening and presymptomatic identification. Significant challenges exist for implementing comprehensive X-ALD newborn screening, including incorporation of the test, coordinating follow-up diagnostic and treatment care, and coordination of extended family testing after case identification.Genet Med 19 1, 121-126.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Tamizaje Neonatal / Adrenoleucodistrofia / Miembro 1 de la Subfamilia D de Transportador de Casetes de Unión al ATP Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies Límite: Female / Humans / Male / Newborn País/Región como asunto: America do norte Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Tamizaje Neonatal / Adrenoleucodistrofia / Miembro 1 de la Subfamilia D de Transportador de Casetes de Unión al ATP Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies Límite: Female / Humans / Male / Newborn País/Región como asunto: America do norte Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos