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Autosomal dominante polyzystische Nierenerkrankung
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Autosomal dominante polyzystische Nierenerkrankung

Klinik: 

Definition: Die autosomal dominanten Zystennieren sind eine Erkrankung des Erwachsenenalters, die durch Mutationen im PKD1- oder PKD2-Gen hervorgerufen werden, und in der hälfte der Fälle zur Dialysepflichtigkeit führt.

 

Systematische Aufstellung weiterführender Links: 

Zystische Nierenerkrankungen
Autosomal dominante polyzystische Nierenerkrankung
PKD1
PKD2
Autosomal rezessive polyzystische Nieren und Lebererkrankung
PKHD1
Branchio-Oto-Renale Dysplasie
Komplex medullärer Zystennierenerkrankungen
MODY5 Diabetes
HNF1B
Nierenzysten und Diabetes (RCAD)
HNF1B

Literatur: 

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