Crigler Najjar Syndrome Type I, A Rare but Severe Cause of Unconjugated Hyperbilirubinemia in Children
Abstract
A rare and severe autosomal recessive disorder of bilirubin metabolism. It has been associated with consanguinity in some patients. Infants without any evidence of hemolysis
Article Information
| Journal | SF Journal of Clinical Case Reports |
| Article Type | Case Report |
| Volume | 1 |
| Issue | 2 |