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

来源：

GINEKOLOGIA POLSKA | 2016年 / 87卷 / 08期

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

页码：605 / 608

页数：4

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