The Liver and Polycystic Kidney Disease

The hereditary forms of polycystic kidney disease (PKD) include a wide range of heterogeneous diseases of great clinical importance, of which autosomal dominant PKD (ADPKD) and autosomal recessive PKD (ARPKD) are the main forms. ADPKD is a multifactorial disorder characterized by bilateral renal cys...

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Bibliografische gegevens

Formaat:	Online
Taal:	Engels
Gepubliceerd in:	Exon Publications 2024
Onderwerpen:	ADPLD Caroli’s disease hepatic cystic dilatations hepatorenal fibrocystic disease polycystic liver disease MJR
Online toegang:	https://directory.doabooks.org/handle/20.500.12854/138173
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