Titlebook: Congenital Adrenal Hyperplasia; Maria I. New,Lenore S. Levine Book 1984 Springer-Verlag Berlin, Heidelberg 1984 Adrenogenitales Syndrom.gl

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,Electron–Specimen Interactions.,traits (Childs et al. 1956; Prader 1958; Wilkins 1962). Males and females are equally at risk (Baulieu et al. 1967). Although there are exceptions (Rosen- bloom and Smith 1966), the clinical presentation—simple virilizing or salt-wasting—is usually consistent within one family. In Europe and the USA

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Enzyme Defects,The following enzymatic deficiencies of steroidogenesis have been described:

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Prenatal Diagnosis,3). Most recently, elevated levels of 17-OHP (Frasier et al. 1975; Nagamani et al. 1978; Hughes and Laurence 1979; Pang et al. 1980b) and Δ. (Pang et al. 1980b) in the amniotic fluid of fetuses affected with CAH due to 21-hydroxylase deficiency have been reported.