KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Management of Polycystic Liver Disease

Savige, Judy, Mallett, Andrew, Tunnicliffe, David J., and Rangan, Gopala K. (2015) KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Management of Polycystic Liver Disease. Seminars in Nephrology, 35 (6). pp. 618-622.

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Abstract

[Extract] Many patients with ADPKD have liver cysts and most are asymptomatic.

Mutations in two different genes account for about 20% of cases with isolated liver cysts (protein kinase C substrate, 80K-H, PRKCSH , and SEC63 , which is a translocation protein SEC63 homologue). In general, patients with ADPKD have fewer and smaller liver cysts than those with isolated PLD, and although liver cysts may predominate, individuals with ADPKD also have renal cysts.

Item ID: 65896
Item Type: Article (Scholarly Work)
ISSN: 1558-4488
Copyright Information: © Elsevier Inc., its licensors, and contributors. All rights reserved.
Date Deposited: 19 Dec 2024 05:15
FoR Codes: 32 BIOMEDICAL AND CLINICAL SCIENCES > 3202 Clinical sciences > 320214 Nephrology and urology @ 100%
SEO Codes: 20 HEALTH > 2001 Clinical health > 200105 Treatment of human diseases and conditions @ 100%
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