Literaturnachweis - Detailanzeige
| Autor/in | Holtzman, Neil A. |
|---|---|
| Institution | Health Services Administration (DHEW/PHS), Rockville, MD. Bureau of Community Health Services. |
| Titel | Newborn Screening for Genetic-Metabolic Diseases: Progress, Principles and Recommendations. |
| Quelle | (1977), (28 Seiten)
PDF als Volltext kostenfreie Datei |
| Dokumenttyp | gedruckt; online; Monographie |
| Schlagwörter | Diseases; Ethics; Infants; Laboratory Techniques; Legal Responsibility; Mental Retardation; Neonates; Organization; Screening Tests |
| Abstract | This monograph, designed for persons involved in the organization and regulation of screening of newborns infants for Phenylketonuria (PKU) and other genetic-metabolic diseases reviews new developments in the field, makes recommendations, and provides information about specific conditions other than PKU that are detectable by screening. Discussed briefly in Part I are various aspects of screening for PKU, ethical and legal issues and screening for other conditions. Part II suggests a model for supervising screening operations for any disorder (from determining what conditions should be screened for, through implementation to evaluation); discusses laboratory responsibilities and offers specific recommendations regarding PKU screening. Part III lists conditions that can be screened for with four different procedures. (SB) |
| Erfasst von | ERIC (Education Resources Information Center), Washington, DC |
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