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Editorial
October 20, 2020

Guidelines for Care of Adults With Down Syndrome

Author Affiliations
  • 1Cincinnati Children’s Hospital Medical Center, Division of Developmental and Behavioral Pediatrics, Division of Adolescent and Transition Medicine, Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio
  • 2Departments of Pediatrics and Medicine, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Northwell Health, Hempstead, New York
  • 3Institute of Health Innovations and Outcomes Research, Feinstein Institutes for Medical Research, Manhasset, New York
  • 4Department of Pediatrics, Indiana University School of Medicine, Indianapolis
  • 5Indiana University School of Medicine Center for Youth and Adults with Conditions of Childhood, Eskenazi Health, Indiana University Health/Riley Hospital for Children, Indianapolis
JAMA. 2020;324(15):1509-1511. doi:10.1001/jama.2020.19150

Down syndrome continues to be the most common chromosomal condition,1,2 with rising prevalence and increased survival. An estimated 1 in 700 infants are born with Down syndrome in the US each year; the median life span is 57 years, with reported survival up to age 82 years.2,3 Improved childhood survival is credited to advances in surgery for congenital heart disease, management of respiratory illness, and decreased institutionalization. Mortality after age 20 years is associated with disorders of the cardiovascular and respiratory systems, with severity of the level of intellectual disability, dementia, and mobility restrictions as important risk factors.3,4

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