Lucey-Driscoll syndrome

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:

Lucey-Driscoll syndrome is an autosomal recessive metabolic disorder affecting enzymes involved in bilirubin metabolism. It is one of several disorders classified as a transient familial neonatal unconjugated hyperbilirubinemia.

The common cause is congenital, but it can also be caused by maternal steroids passed on through breast milk to the newborn. It is different from breast milk jaundice (breast-fed infants have higher bilirubin levels than formula-fed ones).

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A defect in the UGT1A1-gene, also linked to Crigler-Najjar syndrome and Gilbert’s syndrome, is responsible for the congenital form of Lucey-Driscoll syndrome.

• Online Mendelian Inheritance in Man (OMIM) 237900 – transient familial neonatal hyperbilirubinemia, breast feeding jaundice included
• Hyperbilirubinemia, Unconjugated at eMedicine
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