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Autosomal recessive polycystic kidney disease: appearance on fetal MRI

✍ Scribed by Yu-Peng Liu; Sho-Jen Cheng; Shin-Lin Shih; Jon-Kway Huang

Publisher
Springer-Verlag
Year
2005
Tongue
English
Weight
81 KB
Volume
36
Category
Article
ISSN
0301-0449

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## Communicated by Jurgen Horst Autosomal recessive polycystic kidney disease (ARPKD) is an important cause of childhood renal-and liverrelated morbidity and mortality. The clinical spectrum is widely variable. About 30 to 50% of affected individuals die in the neonatal period, while others survive