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Autosomal recessive polycystic kidney disease: improvement of renal function

✍ Scribed by Bettina M. Bosch; Christian Plank; Wolfgang Rascher; Jörg Dötsch


Publisher
Springer
Year
2003
Tongue
English
Weight
164 KB
Volume
162
Category
Article
ISSN
0340-6997

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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