Prenatal ultrasonography of autosomal dominant polycystic kidney disease mimicking recessive type: case series
Author:
Publisher
Springer Science and Business Media LLC
Subject
Radiology Nuclear Medicine and imaging,Pediatrics, Perinatology, and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s00247-018-4325-3.pdf
Reference13 articles.
1. Reeders ST, Breuning MH, Davies KE et al (1985) A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16. Nature 317:542–544
2. Avni FE, Garel C, Cassart M et al (2012) Imaging and classification of congenital cystic renal diseases. AJR Am J Roentgenol 198:1004–1013
3. Brun M, Maugey-Laulom B, Eurin D et al (2004) Prenatal sonographic patterns in autosomal dominant polycystic kidney disease: a multicenter study. Ultrasound Obstet Gynecol 24:5–61
4. Boyer O, Gagnadoux MF, Guest G et al (2007) Prognosis of autosomal dominant polycystic kidney disease diagnosed in utero or at birth. Pediatr Nephrol 22:380–388
5. Audrezet MP, Corbiere C, Lebbah S et al (2016) Comprehensive PKD1 and PKD2 mutation analysis in prenatal autosomal dominant polycystic kidney disease. J Am Soc Nephrol 27:722–729
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