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Cyst fluid composition in human autosomal recessive polycystic kidney disease

✍ Scribed by Rajeev Rohatgi; Beth Zavilowitz; Marcela Vergara; Craig Woda; Paul Kim; Lisa M. Satlin

Publisher
Springer
Year
2004
Tongue
English
Weight
109 KB
Volume
20
Category
Article
ISSN
0931-041X

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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