Practice
Autosomal dominant polycystic kidney disease
Matthew B. Lanktree and Arlene B. Chapman
CMAJ November 13, 2017 189 (45) E1396; DOI: https://doi.org/10.1503/cmaj.170443
Matthew B. Lanktree
Nephrology Division, Department of Medicine (Lanktree), McMaster University, Hamilton, Ont.; Department of Medicine, Section of Nephrology (Chapman), University of Chicago, Chicago, Ill.
MD PhDArlene B. Chapman
Nephrology Division, Department of Medicine (Lanktree), McMaster University, Hamilton, Ont.; Department of Medicine, Section of Nephrology (Chapman), University of Chicago, Chicago, Ill.
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Autosomal dominant polycystic kidney disease
Matthew B. Lanktree, Arlene B. Chapman
CMAJ Nov 2017, 189 (45) E1396; DOI: 10.1503/cmaj.170443
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- Autosomal dominant polycystic kidney disease affects about 1 in 1000 people
- Autosomal dominant polycystic kidney disease is diagnosed by ultrasound
- Supportive care includes management of hypertension, infection and pain
- About 5% of patients will have asymptomatic intracranial aneurysms
- Patients with autosomal dominant polycystic kidney disease should have early referral to a nephrologist
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