Pediatric jaundice liver pigmentation syndrome

Jaundice liver pigmentation syndrome (Dubin-Johnson syndrome) is a disease clinically characterized by intermittent jaundice. The disease is an autosomal dominant hereditary disease with a significant family history. Also known as Dubin-Johnson syndrome, Dubin-Sprinz syndrome, Sprinz-Nelson syndrome, congenital non-hemolytic jaundice, congenital non-hemolytic jaundice type Ⅰ, congenital non-hemolytic jaundice directly increase bilirubin type Ⅰ, Black liver jaundice syndrome.