Multiple cerebral aneurysms in an adult with autosomal recessive polycystic kidney disease
Gately, Ryan, Lock, Gregory, Patel, Chirag, Clouston, John, Hawley, Carmel, and Mallett, Andrew (2021) Multiple cerebral aneurysms in an adult with autosomal recessive polycystic kidney disease. Kidney International Reports, 6 (1). pp. 219-223.
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Abstract
[Extract] Autosomal recessive polycystic kidney disease(ARPKD) is a rare form offibrocystic kidneydisease that affects approximately 1 in 20,000 live births. The classic presentation is with prominenthepatic impairment caused by hepatic fibrosis in addition to renal impairment that is more aggressive than that seen in autosomal dominant polycystic kidney disease (ADPKD). Caroli syndrome is the eponymgiven to the combination of ARPKD, hepatic fibrosis, portal hypertension, and intrahepatic bile duct dilatation. It is seen in ≤50% of cases of ARPKD.
| Item ID: | 66019 |
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| Item Type: | Article (Case Study) |
| ISSN: | 2468-0249 |
| Copyright Information: | © 2020, Published by Elsevier Inc. on behalf of the International Society of Nephrology. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
| Date Deposited: | 22 Jun 2022 03:34 |
| FoR Codes: | 32 BIOMEDICAL AND CLINICAL SCIENCES > 3202 Clinical sciences > 320214 Nephrology and urology @ 50% 32 BIOMEDICAL AND CLINICAL SCIENCES > 3202 Clinical sciences > 320213 Medical genetics (excl. cancer genetics) @ 50% |
| SEO Codes: | 20 HEALTH > 2001 Clinical health > 200101 Diagnosis of human diseases and conditions @ 50% 20 HEALTH > 2001 Clinical health > 200105 Treatment of human diseases and conditions @ 50% |
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