Screening for congenital hypothyroidism in the Netherlands
Screening provides a means for 11filtering disease from the population11, until then unrecognized by patient or physician. In an increasing number of diseases, early detection is helpful in preventing serious consequences, by treatment or by genetic counseling on the recurrence risk of congenital disorders. New developments in the early detection of genetic metabolic diseases and other congenital disorders, which are a frequent cause of infant morbidity and mortality, have proceeded rapidly during the last decades (see Galjaard, 1980). Neonatal screening is one of these developments and contri... Mehr ...
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Dokumenttyp: | doctoralThesis |
Erscheinungsdatum: | 1981 |
Schlagwörter: | Netherlands / children / congenital disorders / hypothyroidism / screening |
Sprache: | Englisch |
Permalink: | https://search.fid-benelux.de/Record/base-26832663 |
Datenquelle: | BASE; Originalkatalog |
Powered By: | BASE |
Link(s) : | http://repub.eur.nl/pub/30696 |