Autosomal dominant polycystic kidney disease diagnosed in utero. Review

被引:4
|
作者
Nowak, Magdalena [1 ]
Huras, Hubert [1 ]
Wiechec, Marcin [1 ]
Jach, Robert [2 ]
Radon-Pokracka, Malgorzata [1 ]
Gorecka, Joanna [1 ]
机构
[1] Jagiellonian Univ, Coll Med, Dept Obstet & Perinatol, Krakow, Poland
[2] Univ Hosp Krakow, Dept Gynecol Endocrinol, Krakow, Poland
关键词
genetic counseling; congenital malformations; magnetic resonance imaging; prenatal diagnostic; prenatal; ultrasonography; autosomal dominant polycystic kidney diseases; DIFFERENTIAL-DIAGNOSIS; PRENATAL-DIAGNOSIS; IN-UTERO; PKD1; GENE; MANIFESTATIONS; ABNORMALITIES; MULTICENTER; PROGRESSION; PROGNOSIS;
D O I
10.5603/GP.2016.0053
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Autosomal dominant polycystic kidney disease (ADPKD) is one of most common inherited renal diseases. It is estimated that very early onset ADPKD affects even 2% patients. The purpose of this article is to provide a comprehensive review of genetics, prenatal diagnosis and prognosis in very early onset autosomal dominant polycystic kidney disease.
引用
收藏
页码:605 / 608
页数:4
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