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MR cholangiography in children with autosomal recessive polycystic kidney disease

✍ Scribed by Gregor Jung; Gabriele Benz-Bohm; Harald Kugel; Klaus-Michael Keller; Uwe Querfeld


Publisher
Springer-Verlag
Year
1999
Tongue
English
Weight
240 KB
Volume
29
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