A rare BSEP mutation associated with a mild form of progressive familial intrahepatic cholestasis type 2

Medicine & Life Sciences

• Acute Liver Failure 15%
• Avitaminosis 17%
• Bile 13%
• Bile Acids and Salts 55%
• Cholestasis 15%
• Fats 10%
• Fibrosis 9%
• Genes 16%
• Genetic Testing 13%
• Hepatocellular Carcinoma 10%
• Hepatocytes 11%
• Heterozygote 14%
• Liver Failure 29%
• Liver Transplantation 12%
• Missense Mutation 13%
• Mutation 29%
• Parents 10%
• Progressive familial intrahepatic 2 Cholestasis 100%
• Proteins 19%
• Pruritus 13%
• Sequence Deletion 15%
• Siblings 48%
• Therapeutics 4%
• Ursodeoxycholic Acid 17%