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Liver disease in autosomal recessive polycystic kidney disease

✍ Scribed by Benjamin L. Shneider; Margret S. Magid


Book ID
110895912
Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
209 KB
Volume
9
Category
Article
ISSN
1397-3142

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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