Congenital polycystic kidney disease complicated by dysplastic kidney in a neonate

HE Ming-Feng; CHEN Ping-Yang; LUO Kai-Ju

doi:10.7499/j.issn.1008-8830.2014.10.022

PDF(1028 KB)

Chinese Journal of Contemporary Pediatrics ›› 2014, Vol. 16 ›› Issue (10) : 1062-1063. DOI: 10.7499/j.issn.1008-8830.2014.10.022

CASE REPORT

Congenital polycystic kidney disease complicated by dysplastic kidney in a neonate

HE Ming-Feng, CHEN Ping-Yang, LUO Kai-Ju

Author information +

History +

Abstract

No abstract available

Cite this article

EndNote

Ris (Procite)

Bibtex

Download Citations

HE Ming-Feng, CHEN Ping-Yang, LUO Kai-Ju. Congenital polycystic kidney disease complicated by dysplastic kidney in a neonate[J]. Chinese Journal of Contemporary Pediatrics. 2014, 16(10): 1062-1063 https://doi.org/10.7499/j.issn.1008-8830.2014.10.022

References

[1] 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.
[5] 王德志, 方元勋, 汪露祥. 新生儿先天性多囊肾合并孤立肾1 例[J]. 罕少疾病杂志, 2003, 10(3): 47.
[6] Büscher R, Büscher AK, Weber S, et al. Clinical manifestationsof autosomal recessive polycystic kidney disease (ARPKD):kidney-related and non-kidney-related phenotypes[J]. PediatrNephrol, 2013: 1-11.
[7] 郑芸, 杨贤卫, 周鑫, 等. 婴儿型多囊肾的影像学诊断[J]. 罕少疾病杂志, 2011, 18(2): 4-7.
[8] Harris PC, Torres VE. Polycystic kidney disease[J]. Annu RevMed, 2009, 60: 321-337.
[9] Krall P, Pineda C, Ruiz P, et al. Cost-effective PKHD1 genetictesting for autosomal recessive polycystic kidney disease[J].Pediatr Nephrol, 2014, 29(2): 223-234.
[10] 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.
[13] 张金哲, 潘少川, 黄澄如. 实用小儿外科学[M]. 杭州：浙江科学技术出版社, 2003: 905.