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citrin/debelost

Povezava se shrani v odložišče
ČlankiKliničnih preskušanjPatenti
3 rezultatov

Chronic hepatitis without hepatic steatosis caused by citrin deficiency in a child.

Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
Citrin deficiency manifests as both neonatal intrahepatic cholestasis (NICCD) during early infancy and adult-onset type II citrullinemia during adulthood. Hepatic steatosis is most frequently observed in patients with citrin deficiency. Thus, non-alcoholic fatty liver disease that is unrelated to

Citrin deficiency as a cause of chronic liver disorder mimicking non-alcoholic fatty liver disease.

Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
OBJECTIVE Citrin deficiency caused by SLC25A13 gene mutations develops into adult-onset type II citrullinemia (CTLN2) and may be accompanied with hepatic steatosis and steatohepatitis. As its clinical features remain unclear, we aimed to explore the characteristics of fatty liver disease associated

Steatogenesis in adult-onset type II citrullinemia is associated with down-regulation of PPARα.

Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
SLC25A13 (citrin or aspartate-glutamate carrier 2) is located in the mitochondrial membrane in the liver and its genetic deficiency causes adult-onset type II citrullinemia (CTLN2). CTLN2 is one of the urea cycle disorders characterized by sudden-onset hyperammonemia due to reduced argininosuccinate
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