Unconjugated hyperbilirubinaemia
Increase in bilirubin
- Polycythaemia – intra-uterine growth retardation, delay cord clamping, twin-twin transfusion syndrome
- Haemolysis – Rhesus, ABO incompatibility, G6PD, phenylketonuria, spheroeliptocytosis, infection
- Sequestered – cephalhaematoma, bruising, intraventricular haemorrhage
- Increased enterohepatic circulation – fasting, delay stooling, swallowed blood, gastrointestinal obstruction
- Drugs – synthetic vitamin K3, oxytocin, naphthalene
Decrease uptake, conjugation, and excretion
- inherited conjugated defects –
- Crigler-Najjar Syndrome types I & II
- Lucey-Driscoll syndrome
- Gilbert’s syndrome
- breast milk
- hypothyroidism
Increase enterohepatic circulation
- intestinal obstruction / delay – e.g. meconium / paralytic ileus

Conjugated hyperbilirubinaemia
Hepatocellular disease
- infections – neonatal sepsis, TORCH
- metabolic – cystic fibrosis, galactosaemia, α-1 antitrypsin deficiency
- prolonged parenteral nutrition
Biliary atresia
- intrahepatic
- extrahepatic
Obstructions
- inspissated bile syndrome
- choledochal cyst