open access

Vol 87, No 8 (2016)
Review paper
Published online: 2016-08-31
Get Citation

Autosomal dominant polycystic kidney disease diagnosed in utero. Review

Magdalena Nowak, Hubert Huras, Marcin Wiecheć, Robert Jach, Małgorzata Radoń-Pokracka, Joanna Górecka
DOI: 10.5603/GP.2016.0053
·
Pubmed: 27629138
·
Ginekol Pol 2016;87(8):605-608.

open access

Vol 87, No 8 (2016)
REVIEW PAPERS Obstetrics
Published online: 2016-08-31

Abstract

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.

Abstract

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.

Get Citation

Keywords

genetic counseling, congenital malformations, magnetic resonance imaging, prenatal diagnostic, prenatal ultrasonography, autosomal dominant polycystic kidney diseases

About this article
Title

Autosomal dominant polycystic kidney disease diagnosed in utero. Review

Journal

Ginekologia Polska

Issue

Vol 87, No 8 (2016)

Article type

Review paper

Pages

605-608

Published online

2016-08-31

DOI

10.5603/GP.2016.0053

Pubmed

27629138

Bibliographic record

Ginekol Pol 2016;87(8):605-608.

Keywords

genetic counseling
congenital malformations
magnetic resonance imaging
prenatal diagnostic
prenatal ultrasonography
autosomal dominant polycystic kidney diseases

Authors

Magdalena Nowak
Hubert Huras
Marcin Wiecheć
Robert Jach
Małgorzata Radoń-Pokracka
Joanna Górecka

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