Polycystic kidney disease medical therapy: Difference between revisions
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==Overview== | ==Overview== | ||
==Treatment== | ==Treatment== | ||
Treatment of ADPKD is targeted at managing symptoms and disease complications. There have been no treatments associated with disease regression or slowing of cysts formation.<ref name="pmid18832246">{{cite journal| author=Grantham JJ| title=Clinical practice. Autosomal dominant polycystic kidney disease. | journal=N Engl J Med | year= 2008 | volume= 359 | issue= 14 | pages= 1477-85 | pmid=18832246 | doi=10.1056/NEJMcp0804458 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=18832246 }} </ref> | |||
===Hypertension=== | |||
===Hematuria=== | |||
===Urinary Tract Infections=== | |||
===Pain=== | |||
===Kidney Stones=== | |||
===Renal Failure=== | |||
==References== | ==References== |
Revision as of 13:14, 25 November 2013
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Steven C. Campbell, M.D., Ph.D. Cafer Zorkun, M.D., Ph.D. [1]
Overview
Treatment
Treatment of ADPKD is targeted at managing symptoms and disease complications. There have been no treatments associated with disease regression or slowing of cysts formation.[1]
Hypertension
Hematuria
Urinary Tract Infections
Pain
Kidney Stones
Renal Failure
References
- ↑ Grantham JJ (2008). "Clinical practice. Autosomal dominant polycystic kidney disease". N Engl J Med. 359 (14): 1477–85. doi:10.1056/NEJMcp0804458. PMID 18832246.