1 he risk of bilirubin encephalopathy (Crigler-Najjar syndrome).

2                                  For Crigler-Najjar syndrome, an inherited disorder that results in f

3  both alleles, whereas patients with Crigler-Najjar syndrome are homozygous for a defect that yields

4 lirubinemia in the Gunn rat model of Crigler-Najjar syndrome can be achieved with one injection of HD

5                                      Crigler-Najjar syndrome (CN) is a very rare genetic disorder cha

6                                      Crigler-Najjar syndrome is a recessively inherited disorder char

7                                      Crigler-Najjar syndrome type 1 (CN-1) is a recessively inherited

8 c bilirubin glucuronidation, causing Crigler-Najjar syndrome type 1 or 2, respectively.

9 perbilirubinemic Gunn rats (model of Crigler-Najjar syndrome type 1) resulted in hUGT1A1 expression i

10                                      Crigler-Najjar syndrome type I is characterized by unconjugated

11  report describes a young adult with Crigler-Najjar syndrome type II in whom kernicterus developed af

12 transplantation in the management of Crigler-Najjar syndrome, type 1.

13  rat is an excellent animal model of Crigler-Najjar syndrome, type 1.

14                         In contrast, Crigler-Najjar syndrome types I and II are rare genetic disorder