[1] Jiang C, Zhou Q, Jin M, et al. Congenital hepatic fibrosis with polycystic kidney disease: Two case reports. Medicine (Baltimore). 2019,98(20):e15600.
[2] 冯茂森,马文斌,汤善宏,等. 先天性肝纤维化的发病机制及诊治现状. 临床肝胆病杂志,2017,33(3):553-557.
[3] 吴燕京,丁惠国. 遗传性多囊肾病:被忽略的肝硬化病因. 中华肝脏病杂志,2016,24(10):728-731.
[4] 常染色体显性多囊肾病临床实践指南专家委员会. 中国常染色体显性多囊肾病临床实践指南(第二版). 临床肾脏病杂志,2019,19(4):227-235.
[5] 曹丽丽,董漪,徐志强,等. 常染色体隐性遗传性多囊肾合并先天性肝纤维化一家系3例报告及文献复习. 临床肝胆病杂志,2019,35(1):166-168.
[6] 杨灿洪,刘志华. 先天性肝纤维化合并多囊肾1例. 中华肝脏病杂志,2015,23(6):467-468.
[7] Chandar J, Garcia J, Jorge L, et al. Transplantation in autosomal recessive polycystic kidney disease: liver and/or kidney? Pediatr Nephrol,2015,30(8):1233-1242. |
