DISORDER
MECHANISM
FEATURES
CLUE
↑ heme breakdown overwhelms conjugation
Unconjugated ↑; ↑ urine urobilinogen; no bilirubinuria
Anemia, ↑ LDH, ↓ haptoglobin, pigment stones
Physiologic neonatal jaundice
Immature UGT1A1 + high RBC turnover + sterile gut (↑ enterohepatic recirculation)
Unconjugated, appears after 24 h, resolves in 1–2 weeks
Jaundice in the first 24 h is pathologic (hemolysis)
Breastfeeding vs breast milk jaundice
Breastfeeding: poor intake → ↑ enterohepatic circulation · breast milk: β-glucuronidase in milk
Breastfeeding: first week · breast milk: after the first week, lasts weeks
Continue feeding; phototherapy if high
Unconjugated bilirubin (lipid-soluble, unbound) crosses the BBB
Deposits in basal ganglia → lethargy, hypotonia, seizures, deafness, choreoathetosis
Phototherapy makes water-soluble isomers; exchange transfusion
Mildly ↓ UGT1A1 activity (promoter variant), ↓ uptake; AR
Mild unconjugated ↑ with fasting, stress, illness, exercise; otherwise normal
Benign · most common inherited hyperbilirubinemia
Absent UGT1A1; AR
Severe unconjugated ↑ in neonates → kernicterus
Phototherapy, plasmapheresis, liver transplant
Severely ↓ (not absent) UGT1A1
Milder; rarely kernicterus
Phenobarbital induces UGT and lowers bilirubin
Defective MRP2 canalicular excretion of conjugated bilirubin; AR
Conjugated ↑; black liver (epinephrine metabolite pigment)
Benign
Defective hepatic uptake and storage (OATP1B1/1B3); AR
Conjugated ↑; normal-colored liver
Milder than Dubin-Johnson, benign
Biliary obstruction (posthepatic)
Stones, pancreatic head cancer, cholangiocarcinoma, strictures, biliary atresia
Conjugated ↑; dark urine, pale stool, pruritus (bile salts), ↑ ALP
↓ urine urobilinogen; fat-soluble vitamin loss