Literature DB >> 16735256

Newborn screening: toward a uniform screening panel and system--executive summary.

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Abstract

The Maternal and Child Health Bureau commissioned the American College of Medical Genetics to outline a process of standardization of outcomes and guidelines for state newborn screening programs and to define responsibilities for collecting and evaluating outcome data, including a recommended uniform panel of conditions to include in state newborn screening programs. The expert panel identified 29 conditions for which screening should be mandated. An additional 25 conditions were identified because they are part of the differential diagnosis of a condition in the core panel, they are clinically significant and revealed with screening technology but lack an efficacious treatment, or they represent incidental findings for which there is potential clinical significance. The process of identification is described, and recommendations are provided.

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Year:  2006        PMID: 16735256     DOI: 10.1542/peds.2005-2633I

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  106 in total

1.  Clinical Preventive Services Coverage and the Affordable Care Act.

Authors:  Jared B Fox; Frederic E Shaw
Journal:  Am J Public Health       Date:  2015-01       Impact factor: 9.308

2.  [Newborn screening as a predictive genetic test: principles and challenges].

Authors:  Johannes Zschocke
Journal:  Wien Med Wochenschr       Date:  2012-03-28

Review 3.  Potential Uses and Inherent Challenges of Using Genome-Scale Sequencing to Augment Current Newborn Screening.

Authors:  Jonathan S Berg; Cynthia M Powell
Journal:  Cold Spring Harb Perspect Med       Date:  2015-10-05       Impact factor: 6.915

4.  Return of Results from Research Using Newborn Screening Dried Blood Samples.

Authors:  Michelle Huckaby Lewis; Aaron J Goldenberg
Journal:  J Law Med Ethics       Date:  2015       Impact factor: 1.718

5.  Parental Views on Expanded Newborn Screening Using Whole-Genome Sequencing.

Authors:  Galen Joseph; Flavia Chen; Julie Harris-Wai; Jennifer M Puck; Charlotte Young; Barbara A Koenig
Journal:  Pediatrics       Date:  2016-01       Impact factor: 7.124

6.  Neonatal mortality and outcome at the end of the first year of life in early onset urea cycle disorders--review and meta-analysis of observational studies published over more than 35 years.

Authors:  Peter Burgard; Stefan Kölker; Gisela Haege; Martin Lindner; Georg F Hoffmann
Journal:  J Inherit Metab Dis       Date:  2015-12-03       Impact factor: 4.982

7.  Newborn screening programmes in Europe; arguments and efforts regarding harmonization. Part 1. From blood spot to screening result.

Authors:  J Gerard Loeber; Peter Burgard; Martina C Cornel; Tessel Rigter; Stephanie S Weinreich; Kathrin Rupp; Georg F Hoffmann; Luciano Vittozzi
Journal:  J Inherit Metab Dis       Date:  2012-05-03       Impact factor: 4.982

8.  Stabilities of hemoglobins A and S in dried blood spots stored under controlled conditions.

Authors:  Barbara W Adam; Dana L Chafin; Victor R De Jesús
Journal:  Clin Biochem       Date:  2013-05-20       Impact factor: 3.281

9.  MALDI-ISD Mass Spectrometry Analysis of Hemoglobin Variants: a Top-Down Approach to the Characterization of Hemoglobinopathies.

Authors:  Roger Théberge; Sergei Dikler; Christian Heckendorf; David H K Chui; Catherine E Costello; Mark E McComb
Journal:  J Am Soc Mass Spectrom       Date:  2015-05-22       Impact factor: 3.109

Review 10.  The genetics of Wilson disease.

Authors:  Irene J Chang; Si Houn Hahn
Journal:  Handb Clin Neurol       Date:  2017
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