open access
Autosomal dominant polycystic kidney disease diagnosed in utero. Review
open access
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.
Keywords
genetic counseling, congenital malformations, magnetic resonance imaging, prenatal diagnostic, prenatal ultrasonography, autosomal dominant polycystic kidney diseases
About this articleTitle
Autosomal dominant polycystic kidney disease diagnosed in utero. Review
Journal
Issue
Article type
Review paper
Pages
605-608
Published online
2016-08-31
Page views
1874
Article views/downloads
7449
DOI
10.5603/GP.2016.0053
Pubmed
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
