Autosomal dominant polycystic kidney disease

descriptionPublicationkeyboard_double_arrow_right Article 12 Nov 2017 English Publisher:CMA Joule Inc.Journal:Canadian Medical Association Journal, volume 189, pages E1396-E1396 (issn: 0820-3946, eissn: 1488-2329,

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Authors: Matthew B, Lanktree; Arlene B, Chapman;

doi: 10.1503/cmaj.170443

pmid: 29133541

pmc: PMC5687928

Autosomal dominant polycystic kidney disease

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Abstract

Mutations in PKD1 or PKD2 cause autosomal dominant polycystic kidney disease, which proceeds to kidney failure in 70% of patients between the fourth and seventh decade of life.[1][1] Signs of autosomal dominant polycystic kidney disease (i.e., numerous cysts and enlargement of the kidneys) may be

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Keywords

Hypertension, Humans, Pain Management, Intracranial Aneurysm, Polycystic Kidney, Autosomal Dominant

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