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Polycystic disease of the liver [PDF]
Hepatology, 2004 Autosomal dominant polycystic disease is genetically heterogeneous with mutations in two distinct genes predisposing to the combination of renal and liver cysts (AD-PKD1 and AD-PKD2) and mutations in a third gene yielding isolated liver cysts (the polycystic liver disease gene).
Gregory T. Everson +2 more
openalex +5 more sources
Clinical manifestation, epidemiology, genetic basis, potential molecular targets, and current treatment of polycystic liver disease [PDF]
Orphanet Journal of Rare DiseasesPolycystic liver disease (PLD) is a rare condition observed in three genetic diseases, including autosomal dominant polycystic liver disease (ADPLD), autosomal dominant polycystic kidney disease (ADPKD), and autosomal recessive polycystic kidney disease (
Amir Ali Mahboobipour +3 more
doaj +2 more sources
Combined liver-kidney transplant in polycystic diseases: a case report [PDF]
Einstein (São Paulo), 2023 Polycystic liver disease, a hereditary pathology, usually manifests as autosomal dominant polycystic kidney disease. The many cysts in the liver cause massive hepatomegaly, majorly affecting the patient’s quality of life. In cases of refractory symptoms,
Olival Cirilo Lucena da Fonseca Neto +7 more
doaj +1 more source
Polycystic liver disease [PDF]
Revista Española de Enfermedades Digestivas, 2009 A 54-year-old man had an asymptomatic elevation of cytolysis-related enzymes, GGT, and alkaline phosphatase, detected at a routine laboratory study. The patient reported no alcohol abuse, no history of liver disease, and no constitutional syndrome. Physical examination showed a good general status, normal colored skin and mucosas, and no stigmata of ...
A. Sánchez Cantos +5 more
openaire +5 more sources
Polycystic Liver Disease: A Case Report
The Indonesian Journal of Gastroenterology, Hepatology and Digestive Endoscopy, 2021 Polycystic liver disease is characterized by multiple cystic lesions on the liver. Liver cysts are typically incidental findings, with occasional complications including cyst hemorrhage, infection and rupture.
Randy Adiwinata +10 more
doaj +1 more source
BMC Medicine, 2023 Background Recent studies found associations between non-alcoholic fatty liver disease (NAFLD) and polycystic ovary syndrome (PCOS), but the causal nature of this association is still uncertain.
Dong Liu +8 more
semanticscholar +1 more source
Polycystic liver disease: an overview of clinical manifestations, diagnosis, and treatment [PDF]
Kosin Medical Journal, 2023 Polycystic liver disease (PLD) is a hereditary disease characterized by the presence of 20 or more liver cysts. It is classified into three types: isolated autosomal dominant PLD, PLD with autosomal dominant polycystic kidney disease, and PLD with ...
Joonho Jeong, Hyun Joon Park
doaj +1 more source
Journal of Clinical Medicine, 2023 Background: The metabolic effects of polycystic ovary syndrome (PCOS) may increase the risk of non-alcoholic fatty liver disease (NAFLD). However, the burden of NAFLD in PCOS has not been unequivocally defined. This systematic review (SR), meta-analysis (
R. Manzano-Nuñez +7 more
semanticscholar +1 more source
A SEC61A1 variant is associated with autosomal dominant polycystic liver disease
Liver international (Print), 2022 Autosomal dominant polycystic liver and kidney disease is a spectrum of hereditary diseases, which display disturbed function of primary cilia leading to cyst formation. In autosomal dominant polycystic kidney disease a genetic cause can be determined in
B. Schlevogt +10 more
semanticscholar +1 more source
Journal of Clinical Medicine, 2023 The aim of this case–control study was to assess the burden of non-alcoholic fatty liver disease (NAFLD) in adolescents with polycystic ovary syndrome (PCOS) and its associations with insulin resistance, hyperandrogenism, and other metabolic ...
A. Giannouli +8 more
semanticscholar +1 more source