Dubin-Johnson syndrome

Dubin-Johnson syndrome (DJS) is a benign, inherited liver disorder characterized clinically by chronic, predominantly conjugated, hyperbilirubinemia and histopathologically by black-brown pigment deposition in parenchymal liver cells.

Also known as: Dubin Johnson Syndrome, Dubin-Johnson syndrome, Dubin-Sprinz disease, Sprinz-Nelson syndrome, chronic idiopathic jaundice, hyperbilirubinemia type 2, DJS, conjugated hyperbilirubinemia

0 clinical trials for this condition and its sub-types, 0 tagged with Dubin-Johnson syndrome itself.