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Clinical manifestations of autosomal recessive polycystic kidney disease (ARPKD): kidney-related and non-kidney-related phenotypes

✍ Scribed by Büscher, Rainer; Büscher, Anja K.; Weber, Stefanie; Mohr, Julia; Hegen, Bianca; Vester, Udo; Hoyer, Peter F.

Book ID
121616717
Publisher
Springer
Year
2013
Tongue
English
Weight
854 KB
Volume
29
Category
Article
ISSN
0931-041X

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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