Kidney injury is frequently seen in patients with end‐stage liver disease from cirrhosis and
liver failure. Among selected patients, simultaneous liver kidney (SLK) transplantation …

Autosomal recessive polycystic kidney disease (ARPKD) is a rare but highly relevant
disorder in pediatric nephrology. This genetic disease is mainly caused by variants in the …

Autosomal recessive polycystic kidney disease (ARPKD) is a severe pediatric hepatorenal
disorder with pronounced phenotypic variability. A substantial number of patients with early …

Autosomal recessive polycystic kidney disease–PKHD1 (ARPKD-PKHD1) is characterized
by primary involvement of the kidneys and liver with mostly secondary effects seen in other …

Combined and sequential liver–kidney transplantation (CLKT and SLKT) is a definitive
treatment in children with end-stage organ failure. There are two major indications:-terminal …

Ciliopathies encompass a broad spectrum of diseases stemming from dysfunction of the
primary (non-motile) cilia, present on almost all cells in the human body. These disorders …

Autosomal recessive polycystic kidney disease (ARPKD) is the rare and usually early-onset
form of polycystic kidney disease with a typical clinical presentation of enlarged cystic …

Background Autosomal recessive polycystic kidney disease (ARPKD) is a rare ciliopathy
characterized by congenital hepatic fibrosis and cystic kidney disease. Lack of data about …

Purpose Autosomal recessive polycystic kidney disease (ARPKD) is a hereditary condition
characterized by massive kidney enlargement and developmental liver defects. Potential …

Background Autosomal recessive polycystic kidney disease (ARPKD) with congenital
hepatic fibrosis (CHF) causes portal hypertension and its complications. A transjugular …