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Cystenyrer

Cystenyrer er en arvelig sykdom. Den medisinske betegnelsen er autosomal dominant polycystisk nyresykdom, forkortet ADPKD.

Cystenyrer gir i de fleste tilfeller ingen symptomer i barndom og ungdom. Tilstanden utvikler seg gjerne i 30-50 årsalderen.

Sist oppdatert:

24. mars 2021

Dette dokumentet er basert på det profesjonelle dokumentet Polycystisk nyresykdom . Referanselisten for dette dokumentet vises nedenfor

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  3. Chapman AB. Cystic disease in women: clinical characteristics and medical management. Adv Ren Replace Ther 2003; 10: 24-30. PubMed
  4. Grantham JJ, Chapman AB, Torres VE. Volume progression in autosomal dominant polycystic kidney disease: the major factor determining clinical outcomes. Clin J Am Soc Nephrol 2006; 1: 148-57. PubMed
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  7. Demetriou K, Tziakouri C, Anninou Ket al. Autosomal dominant polycystic kidney disease - type 2. Ultrasound, genetic and clinical correlations. Nephrol Dial Transpl 2000; 15: 205-11. PubMed
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  18. Wüthrich RP, Mei C. Pharmacological management of polycystic kidney disease. Expert Opin Pharmacother 2014; 15: 1085-95. doi:10.1517/14656566.2014.903923 DOI
  19. James PA, Oparil S, Carter BL, et al. 2014 evidence-based guideline for the management of high blood pressure in adults: report from the panel members appointed to the Eighth Joint National Committee (JNC 8). JAMA. 2014;311(5):507–520.
  20. Patch C, Charlton J, Roderick PJ, Gulliford MC. Use of antihypertensive medications and mortality of patients with autosomal dominant polycystic kidney disease: a population-based study. Am J Kidney Dis. 2011 Jun. 57(6):856-62.
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