ABCC2 AR unreviewed
Dubin-Johnson syndrome
Bilirubin excretion
Enzyme or protein defect
MRP2 canalicular transporter
Accumulates or becomes deficient
Conjugated bilirubin
Key features
Conjugated hyperbilirubinaemia; grossly black liver
Management
Benign; reassurance
Not clinical guidance. Written from standard clinical biochemistry, not from the uploaded documents, and marked unreviewed. Teaching-level reference for study and database seeding only. It must not be used to manage a patient.
Recent literature
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