The 20 Best Progressive Familial Intrahepatic Cholestasis Type 3 Doctors Near Me in Hamburg, NY

Progressive familial intrahepatic cholestasis type 3 (PFIC3) is a rare condition that affects the liver. People with this condition generally develop signs and symptoms during late infancy or early childhood, which may include severe itching, jaundice, failure to thrive, portal hypertension (high blood pressure in the vein that provides blood to the liver) and hepatosplenomegaly (enlarged liver and spleen). The condition may progress to liver failure during childhood or adulthood. PFIC3 is caused by change in the ABCB4 gene and is inherited in an autosomal recessive manner.