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Dialyse aktuell 2019; 23(05): 202-203
DOI: 10.1055/a-0886-1252
DOI: 10.1055/a-0886-1252
Expertentipp
Autosomal-dominante polyzystische Nierenerkrankung (ADPKD)
Tolvaptan als erste gezielte Therapie bei polyzystischer NierenerkrankungFurther Information
Publication History
Publication Date:
19 June 2019 (online)
![](https://www.thieme-connect.de/media/dialyseakt/201905/lookinside/thumbnails/10-1055-a-0886-1252-1.jpg)
Die autosomal-dominante polyzystische Nierenerkrankung (ADPKD) ist die häufigste zu einer terminalen Niereninsuffizienz führende genetische Erkrankung. Bis zu 10 % aller europäischen DialysepatientInnen leiden an einer ADPKD [1].
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Literatur
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- 2 Chapman AB, Devuyst O, Eckardt KU. et al. Autosomal-dominant polycystic kidney disease (ADPKD): executive summary from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference. Kidney Int 2015; 88: 17-27 doi:10.1038/ki.2015.59
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