Retrospective Study
Copyright ©The Author(s) 2016.
World J Gastroenterol. May 28, 2016; 22(20): 4901-4907
Published online May 28, 2016. doi: 10.3748/wjg.v22.i20.4901
Table 1 Clinical, laboratory findings and mutations of five infants with progressive familial intrahepatic cholestasis
PatientSexAge of symptom onsetAge at LTxAssociated signAST/ALT (IU/L)(0-37/0-41)T/D. bil (mg/dL)(0-1.2/0-0.5)GGT (IU/L)(6-71)AFP (ng/mL)(0-7.0)Mutations of ABCB11
1F20 d24 moGallstone, HCC602/24211.3/7.9293070S226L/
2F9 mo10 yrGallstone178/2428.2/5.225< 5G776R
3M5 d6 mo-416/9335.1/142521500No
4M1 mo3.5 mo-1467/25044.5/25.150-No
5M2 mo--951/67714.3/8.052770000No