ARPKD and ADPKD

descriptionPublicationkeyboard_double_arrow_right Article 01 Mar 2008 English Publisher:Ovid Technologies (Wolters Kluwer Health)Journal:Journal of the American Society of Nephrology, volume 19, pages 416-418 (issn: 1046-6673,

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Authors: Jun-ya Kaimori; Gregory G. Germino;

doi: 10.1681/asn.2008010033

ARPKD and ADPKD

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Abstract

Superficially, autosomal dominant polycystic kidney disease (ADPKD) and autosomal recessive polycystic kidney disease (ARPKD) seem to be more different than alike. ADPKD is common, its cysts arise from any nephron segment, and it is slowly progressive.[1][1] Hepatic cysts are its primary extrarenal

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Johns Hopkins University
United States

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