Polycystic liver disease: pathophysiology, diagnosis and treatment

LF Norcia, EM Watanabe… - Hepatic Medicine …, 2022 - Taylor & Francis
Polycystic liver disease (PLD) is a clinical condition characterized by the presence of more
than 10 cysts in the liver. It is a rare disease Of genetic etiology that presents as an isolated …

Case report: Rare genetic liver disease-a case of congenital hepatic fibrosis in adults with autosomal dominant polycystic kidney disease

Y Liu, P Zhu, J Tian - Frontiers in Medicine, 2024 - frontiersin.org
Congenital hepatic fibrosis (CHF) is considered to be a rare autosomal recessive hereditary
fibrocystic liver disease, mainly found in children. However, cases of adult CHF with …

The role of exception points in outcomes of patients with fibrocystic liver-kidney disease: Implications for the National Liver Review Board

BE Rosenthal, PL Abt, KR Reddy… - Liver …, 2024 - journals.lww.com
To the editor, Fibrocystic liver-kidney disease (FLKD) results from genetic mutations
involving ciliary function, most often the PKHD1 gene causing autosomal recessive …

Severe polycystic liver disease in a cat

EM King, M Pappano, SK Lorbach… - Journal of Feline …, 2023 - journals.sagepub.com
Case summary Ductal plate malformations (DPMs) are poorly documented in the veterinary
literature, particularly those of the polycystic liver disease (PCLD) phenotype. A 13-year-old …

Nephronophthisis 13 caused by WDR19 variants with pancytopenia: case report

Y Tanaka, T Horinouchi, Y Inoki, Y Ichikawa, C Ueda… - CEN Case Reports, 2024 - Springer
We present a case of nephronophthisis 13 that resulted from WDR19 variants. The patient, a
nine-year-old Japanese boy, had detection of mild proteinuria during a school urine …

Quistes hepáticos

MR Verdyguer, BM Muñoz, FJM Gómez… - Medicine-Programa de …, 2024 - Elsevier
Cystic hepatic lesions encompass a broad, heterogeneous group of lesions with varying
etiology and cell lineage, including simple liver cysts, polycystic liver disease, common bile …

[HTML][HTML] Caroli Disease

B Kyalwazi, P Kudaravalli, S John - europepmc.org
Caroli Disease Beverly Kyalwazi; Pujitha Kudaravalli; Savio John. Author Information Last
Update: August 16, 2024. Continuing Education Activity Caroli disease is a rare, congenital …