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transient familial neonatal hyperbilirubinemia

Pathology: - one or more components in the milk may trigger the jaundice in infants who have such mutations Genetics: - associated with defects in UGT1A1 gene - mutations are identical to those detected in patients with Gilbert syndrome Clinical manifestations: - hyperbilirubinemia may lead to jaundice - breast milk jaundice is a common problem in nursing infants - may result in prolonged unconjugated hyperbilirubinemia associated with breast milk

General

neonatal hyperbilirubinemia genetic disease

Database Correlations

OMIM 237900

References

OMIM :accession 237900