HE Ming-Feng,CHEN Ping-Yang,LUO Kai-Ju. Congenital polycystic kidney disease complicated by dysplastic kidney in a neonate[J]. CJCP, 2014, 16(10): 1062-1063.
Lau EC, Janson MM, Roesler MR, et al. Birth of a healthy infantfollowing preimplantation PKHD1 haplotyping for autosomalrecessive polycystic kidney disease using multiple displacementamplification[J]. J Assist Reprod Genet, 2010, 27(7): 397-407.
[2]
Zhou XH, Hui ZY, Li Y. Clinical and pathological features ofa neonate with autosomal recessive polycystic kidney diseasecaused by a nonsense PKHD1 mutation[J]. World J Pediatr,2013, 9(1): 76-79.
[3]
Smith JM, McDonald RA. Autosomal recessive polycystickidney disease[M]//Fibrocystic Diseases of the Liver. New York:Humana Press, 2010: 319-330.
[4]
Sweeney WE Jr, Avner ED. Diagnosis and management ofchildhood polycystic kidney disease[J]. Pediatr Nephrol, 2011,26(5): 675-692.
Aytaç B, Seh?toğlu I, Vuruskan H. Multicystic dysplastic kidney:four-year evaluation[J]. Turk Patoloji Derg, 2011, 27(3): 210-214.
[11]
Cooper CJ, Said S, Khalillullah S, et al. Multicystic dysplastickidney complicated by pyelonephritis[J]. Am J Case Rep,2013,14: 412-415.
[12]
Mei H, Qi T, Li S , et al. Transumbilical multiport laparoscopicnephroureterectomy for congenital renal dysplasia in children:midterm follow-up from a single institution[J]. Front Pediatr,2013, 1: 46.