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Titlebook: Neonatal Screening for Inborn Errors of Metabolism; Horst Bickel,Robert Guthrie (Professor of Pediatri Conference proceedings 1980 Springe

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Newborn Screening for Maple Syrup Urine Disease (Branched-Chain Ketoaciduria) is usually rapid with development of neurologic manifestations, convulsions, coma, and death. Untreated or improperly treated infants who survive will generally have severe mental and motor retardation.
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Newborn Screening for Inherited Disorders of Galactose Metabolism978). Since then, the technique of screening has been diversified, two new defects of galactose metabolism have been discovered (Gitzelmann 1965, 1972), and a number of transferase variant enzymes have been described.
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Neonatal Screening for Hypothyroidism in Brussels in children in Holland (De Jonge 1977) and Sweden (Aim et al. 1978). Our results are very different. In a population of about 5000 newborns, we have established the diagnosis of hypothyroidism in 12, an incidence of approximately 1:500. This figure is thus six to ten times higher than that reported by the other groups.
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fficient preventive pediatrics. At present, routine neonatal screening covering a satisfactory percentage of newborn babies is carried out in only a small part ofthe world. For some five diseases enough infants have been screened to give reasonably reliable information about the frequency of these d
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Significance and Need of Screening for Hyperlipidemia in Childhood. 1960; Keys et al. 1963), which have now clearly established that the increase of certain lipid and lipoprotein fractions of plasma must be considered as a major risk factor predicting morbid events related to atherosclerotic disease.
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