Several metabolic monogenic diseases may be cured by liver transplantation alone (LTA) or by combined liver–kidney transplantation (CLKT) when the metabolic disease has caused end-stage renal disease. Liver transplantation may be regarded as a substitute for an injured liver or as supplying a tissue that may replace a mutant protein. Two groups of diseases should be distinguished. In the first group, the kidney tissue may be severely damaged while the liver tissue is almost normal. In this group, renal transplantation is recommended according to the degree of renal damage and liver transplantation is essential as a genetic therapy for correcting the metabolic disorder. In the second group, the liver parenchymal damage is severe. In this gro...
Autosomal dominant polycystic kidney disease ADPKD is a rare disorder, characterized by multiple m...
The liver and kidneys are often similarly affected by a single disease. This is the case in metaboli...
Introduction: In primary hyperoxaluria type 1 (PH1), oxalate overproduction frequently causes kidney...
Several metabolic monogenic diseases may be cured by liver transplantation alone (LTA) or by combine...
While the prevalence of most diseases caused by single-gene mutations is low and defines them as rar...
SummaryWhile the prevalence of most diseases caused by single-gene mutations is low and defines them...
Acute or chronic liver failure is commonly associated with some degree of renal dysfunction. In sele...
Glycogen storage disease type la (GSD la) is a rare metabolic disorder due to hepatic glucose-6-phos...
Objective Adult Polycystic liver disease (PLD) is frequently associated with autosomal dominant poly...
Polycystic disease causes a progressive decrease in renal function and liver degeneration. The progr...
The experience of combined liver-kidney transplantation (CLKT) is limited in pediatric populations. ...
Background. Renal insufficiency is increasingly common in end-stage liver disease and allocation of ...
Primary hyperoxaluria type 1 is an autosomal recessive hereditary glyoxylate metabolism disorder cha...
The new Organ Procurement and Transplant Network/United Organ Sharing Network (OPTN/UNOS) simultaneo...
Introduction: MMA is a rare autosomal recessive disorder with the manifestation of recurrent and sev...
Autosomal dominant polycystic kidney disease ADPKD is a rare disorder, characterized by multiple m...
The liver and kidneys are often similarly affected by a single disease. This is the case in metaboli...
Introduction: In primary hyperoxaluria type 1 (PH1), oxalate overproduction frequently causes kidney...
Several metabolic monogenic diseases may be cured by liver transplantation alone (LTA) or by combine...
While the prevalence of most diseases caused by single-gene mutations is low and defines them as rar...
SummaryWhile the prevalence of most diseases caused by single-gene mutations is low and defines them...
Acute or chronic liver failure is commonly associated with some degree of renal dysfunction. In sele...
Glycogen storage disease type la (GSD la) is a rare metabolic disorder due to hepatic glucose-6-phos...
Objective Adult Polycystic liver disease (PLD) is frequently associated with autosomal dominant poly...
Polycystic disease causes a progressive decrease in renal function and liver degeneration. The progr...
The experience of combined liver-kidney transplantation (CLKT) is limited in pediatric populations. ...
Background. Renal insufficiency is increasingly common in end-stage liver disease and allocation of ...
Primary hyperoxaluria type 1 is an autosomal recessive hereditary glyoxylate metabolism disorder cha...
The new Organ Procurement and Transplant Network/United Organ Sharing Network (OPTN/UNOS) simultaneo...
Introduction: MMA is a rare autosomal recessive disorder with the manifestation of recurrent and sev...
Autosomal dominant polycystic kidney disease ADPKD is a rare disorder, characterized by multiple m...
The liver and kidneys are often similarly affected by a single disease. This is the case in metaboli...
Introduction: In primary hyperoxaluria type 1 (PH1), oxalate overproduction frequently causes kidney...