Case Report: A rare case of familial progressive cholestasis type 10 in an adult with heterozygous MYO5B variant
{{output}}
Progressive familial intrahepatic cholestasis (PFIC) is a group of rare autosomal recessive cholestatic liver diseases that typically manifest in infancy or childhood. It is characterized by intrahepatic cholestasis, jaundice, pruritus, and malabsorption, with... ...
