Sök artiklar i SveMed+

Observera: SveMed+ upphör att uppdateras!



Autosomal dominant polycystisk nyresygdom
Engelsk titel: Autosomal dominant polycystic kidney disease Läs online Författare: Naver, Signe Vinsand ; Örskov, Bjarne ; Möller Jensen, Anja ; Egfjord, Martin Språk: Dan Antal referenser: 29 Dokumenttyp: Översikt UI-nummer: 18010203

Tidskrift

Ugeskrift for Laeger 2017;179(20)1751-5 ISSN 0041-5782 E-ISSN 1603-6824 KIBs bestånd av denna tidskrift Denna tidskrift är expertgranskad (Peer-Reviewed)

Sammanfattning

Autosomal dominant polycystic kidney disease (ADPKD) is the most common genetic disorder which causes end stage renal disease. In Denmark, estimated 5,000 patients are living with the disease. Most of the patients are in regular contact with physicians due to the progression of kidney failure causing hypertension as well as cyst infections, back pain, abdominal distension and other symptoms caused by the enlarged kidneys. In this article we describe the clinical presentation, the genetics, the pathophysiology and the current and future treatment modalities of the disease.