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Prenatal diagnosis of autosomal recessive polycystic kidney disease by molecular genetic analysis

✍ Scribed by Dong Gyu Jang; Hyojin Chae; Jong Chul Shin; In Yang Park; Myungshin Kim; Yonggoo Kim

Book ID
109007644
Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
206 KB
Volume
37
Category
Article
ISSN
1341-8076

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Autosomal recessive polycystic kidney disease (ARPKD) is one of the most common hereditary renal cystic diseases and has a high infant mortality. Prenatal diagnosis using fetal sonography can be unreliable, especially in early pregnancy. The ARPKD locus has been mapped to proximal chromosome 6p allo

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## Communicated by Jurgen Horst Autosomal recessive polycystic kidney disease (ARPKD) is one of the most common hereditary renal cystic diseases in children. The clinical spectrum ranges from stillbirth and neonatal demise to survival into adulthood. In a given family, however, patients usually di