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DS-Connect: A Promising Tool to Improve Lives and Engage Down Syndrome Communities Worldwide.
Peprah, Emmanuel K; Parisi, Melissa A; Kaeser, Lisa; Bardhan, Sujata; Oster-Granite, MaryLou; Maddox, Yvonne T.
Afiliação
  • Peprah EK; Center for Translation Research and Implementation Science, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD, USA. Electronic address: peprahek@mail.nih.gov.
  • Parisi MA; Intellectual and Developmental Disabilities Branch, Eunice Shriver Kennedy National Institute for Child Health and Human Development, National Institutes of Health, Bethesda, MD, USA.
  • Kaeser L; Office of Legislation and Public Policy, Eunice Shriver Kennedy National Institute for Child Health and Human Development, National Institutes of Health, Bethesda, MD, USA.
  • Bardhan S; Intellectual and Developmental Disabilities Branch, Eunice Shriver Kennedy National Institute for Child Health and Human Development, National Institutes of Health, Bethesda, MD, USA.
  • Oster-Granite M; Intellectual and Developmental Disabilities Branch, Eunice Shriver Kennedy National Institute for Child Health and Human Development, National Institutes of Health, Bethesda, MD, USA.
  • Maddox YT; National Institute on Minority Health and Health Disparities, National Institutes of Health, Bethesda, MD, USA.
Glob Heart ; 10(4): 337-40, 2015 Dec.
Article em En | MEDLINE | ID: mdl-26271554
ABSTRACT
Down syndrome (DS) is the most common genetic cause of intellectual and developmental disabilities in the United States with an estimated birth prevalence of 1691 births; however, worldwide estimates of the number of individuals with intellectual and developmental disabilities, including DS, remain speculative. Little is known about the global health impact of DS, such as heart defects, gastrointestinal malformations, and other medical and behavioral issues. Further research is needed to develop the next generation of novel therapies and compounds aimed at improving cognition, reducing dementia, and mitigating other manifestations of DS. To address these challenges, the National Institutes of Health has created the first web-based, voluntary registry and data resource called DS-Connect The Down Syndrome Registry to collect demographic and health information about individuals with DS.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prevalence_studies / Risk_factors_studies Limite: Adult / Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prevalence_studies / Risk_factors_studies Limite: Adult / Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article