Choose one of the five choices you want to search:

Gene, Transcriptome, Protein, Pathway or Disease. 

"Lucey-Driscoll syndrome" information

LiverAtlas Disease IDHuLDi00147
NameLucey-Driscoll syndrome
DescriptionThe 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).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. Xref: URL
DefinitionLucey-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. Xref: URL
XrefClinical Hepatology,2004.Page 585
UMLS2011AA:C0270210
Genetics RelationGene/Protein/Pathway
Gene:UGT1A1
Protein: