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Other Names for this Disease
- Transient familial hyperbilirubinemia
- Transient familial neonatal hyperbilirubinemia
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transient familial hyperbilirubinemia, is a rare metabolic disorder that leads to very high levels of bilirubin in a newborn's blood. Babies with this disorder may be born with severe jaundice (yellow skin), yellow eyes and lethargy. It occurs when the body does not properly break down (metabolize) a certain form of bilirubin. If untreated, this condition can cause seizures, neurologic problems (kernicterus) and even death. Treatment for Lucey-Driscoll syndrome includes phototherapy with blue light (to treat the high level of bilirubin in the blood) and an exchange transfusion is sometimes necessary. Different inheritance patterns have been reported and in some cases, it occurs in individuals with no family history of the condition.Lucey-Driscoll syndrome, a form of
Last updated: 11/15/2010
- Diana Chambers, David Zieve. Transient familial hyperbilirubinemia. MedlinePlus. August 11, 2009; http://www.nlm.nih.gov/medlineplus/ency/article/001196.htm. Accessed 11/8/2010.
- Genetics Home Reference (GHR) contains information on Lucey-Driscoll syndrome. This website is maintained by the National Library of Medicine.
- MedlinePlus was designed by the National Library of Medicine to help you research your health questions, and it provides more information about this topic. Click on the link to view this information.
In Depth Information
- The Online Mendelian Inheritance in Man (OMIM) database contains genetics resources that discuss Lucey-Driscoll syndrome. Click on the link to go to OMIM and review these resources.
- Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.
- PubMed is a searchable database of medical literature and lists journal articles that discuss Lucey-Driscoll syndrome. Click on the link to view a sample search on this topic.