| 11. | Type II citrullinemia may also develop in people who had a liver disorder called neonatal cholestasis during infancy.
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| 12. | Citrin is associated with type II citrullinemia and neonatal intrahepatic cholestasis caused by citrin deficiency ( NICCD ).
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| 13. | This protein is associated with progressive familial intrahepatic cholestasis type 1 as well as benign recurrent intrahepatic cholestasis.
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| 14. | This protein is associated with progressive familial intrahepatic cholestasis type 1 as well as benign recurrent intrahepatic cholestasis.
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| 15. | Cholestasis, Stevens Johnson syndrome, and toxic epidermal necrolysis are some other rare side effects that may occur.
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| 16. | Low levels of albumin tend to indicate a chronic condition, while it is normal in hepatitis and cholestasis.
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| 17. | A diameter of more than 8 mm is regarded as abnormal dilatation, and is a sign of cholestasis.
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| 18. | Mutations in this gene may result in progressive familial intrahepatic cholestasis type 1 and in benign recurrent intrahepatic cholestasis.
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| 19. | Mutations in this gene may result in progressive familial intrahepatic cholestasis type 1 and in benign recurrent intrahepatic cholestasis.
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| 20. | In the liver, the enlargement of hepatocytes due to fatty change may compress adjacent bile canaliculi, leading to cholestasis.
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