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Alternative NamesLucey-Driscol syndrome
Definition Return to top
Transient familial hyperbilirubinemia is a metabolic disorder passed down through families. Babies with this disorder are born with severe jaundice.
Causes Return to top
Transient familial hyperbilirubinemia is thought to be an autosomal recessive inherited disorder. It occurs when the body does not properly break down (metabolize) a certain form of bilirubin. Bilirubin levels rapidly build up in the body. The high levels are poisonous to the brain and can cause death.
Symptoms Return to top
The newborn may have:
If untreated, seizures and neurologic problems (kernicterus) may develop.
Exams and Tests Return to top
Blood tests for bilirubin levels can identify the severity of the jaundice.
Treatment Return to top
Phototherapy with blue light is used to treat the high level of bilirubin. An exchange transfusion is sometimes necessary.
Outlook (Prognosis) Return to top
Babies who are treated can have a good outcome. If the condition is not treated, severe complications develop. This disorder tends to improve with time.
Possible Complications Return to top
Death or severe neurological deficits can occur if the condition is not treated.
When to Contact a Medical Professional Return to top
Although this problem would most likely be noted immediately after delivery, call your doctor if you notice your baby's skin turning yellow. There are other causes for jaundice in the newborn that are easily treated.
Prevention Return to top
Phototherapy can significantly prevent the potentially serious complications of this disorder.Update Date: 7/25/2007 Updated by: Chad Haldeman-Englert, MD, Division of Human Genetics, Children's Hospitalof Philadelphia, Philadelphia, PA. Review provided by VeriMed HealthcareNetwork.