Bilirubin levels greater than 10x normal could indicate neoplastic or intrahepatic cholestasis.
2.
Citrin is associated with type II citrullinemia and neonatal intrahepatic cholestasis caused by citrin deficiency ( NICCD ).
3.
This protein is associated with progressive familial intrahepatic cholestasis type 1 as well as benign recurrent intrahepatic cholestasis.
4.
This protein is associated with progressive familial intrahepatic cholestasis type 1 as well as benign recurrent intrahepatic cholestasis.
5.
Mutations in this gene may result in progressive familial intrahepatic cholestasis type 1 and in benign recurrent intrahepatic cholestasis.
6.
Mutations in this gene may result in progressive familial intrahepatic cholestasis type 1 and in benign recurrent intrahepatic cholestasis.
7.
Genetic mutations affecting hepatic bile salt transport molecules have also been found in patients with progressive familial intrahepatic cholestasis ( PFIC ).
8.
The corresponding protein in mice is essential for the development of B cells and red blood cells, and for the prevention of intrahepatic cholestasis.
9.
Often testing will be done to exclude more common conditions that present in a similar fashion, including intrahepatic cholestasis of pregnancy, and autoimmune hepatitis.
10.
Researchers have found many infants with neonatal intrahepatic cholestasis have the same mutations in the " SLC25A13 " gene as adults with type II citrullinemia.
