Zusammenfassung
Im Gegensatz zum zentralen Diabetes insipidus (S. 203), der schon 1674 als selbständige Erkrankung abgegrenzt wurde, ist der erbliche nephrogene Diabetes insipidus erst seit 15 Jahren bekannt. Er wurde 1945 gleichzeitig in Schweden (7) und in den USA (23) beschrieben und in Deutschland erstmalig 1956 (18) beobachtet.
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Buchborn, E. (1960). Familiärer nephrogener Diabetes insipidus. In: Linneweh, F. (eds) Die Prognose Chronischer Erkrankungen / Long-Term Observations of Chronic Diseases. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-92788-1_27
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