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Long-term follow-up after diagnosis resulting from newborn screening: statement of the US Secretary of Health and Human Services' Advisory Committee on Heritable Disorders and Genetic Diseases in Newborns and Children

Authors :
Julie Miller
Christopher A. Kus
Alan R. Hinman
Coleen A. Boyle
Brad Therrell
R. Rodney Howell
Carol L. Greene
James Figge
Alex R. Kemper
Derek Robertson
Jill L Fisch
Javier Aceves
Michele A. Lloyd-Puryear
Denise Dougherty
Peter C. van Dyck
Source :
Genetics in medicine : official journal of the American College of Medical Genetics. 10(4)
Publication Year :
2008

Abstract

The US Secretary of Health and Human Services' Advisory Committee on Heritable Disorders and Genetic Diseases in Newborns and Children provides guidance to reduce the morbidity and mortality associated with heritable disorders, with a special emphasis on those conditions detectable through newborn screening. Although long-term follow-up is necessary to maximize the benefit of diagnosis through newborn screening, such care is variable and inconsistent. To begin to improve long-term follow-up, the Advisory Committee has identified its key features, including the assurance and provision of quality chronic disease management, condition-specific treatment, and age-appropriate preventive care throughout the lifespan of affected individuals. There are four components central to achieving long-term follow-up: care coordination through a medical home, evidence-based treatment, continuous quality improvement, and new knowledge discovery.

Details

ISSN :
15300366
Volume :
10
Issue :
4
Database :
OpenAIRE
Journal :
Genetics in medicine : official journal of the American College of Medical Genetics
Accession number :
edsair.doi.dedup.....c52dd960ee2a752e21de9a9c9450c4fe