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Autosomal recessive polycystic kidney disease

✍ Scribed by Bernard S. Kaplan; J. Fay; Vanita Shah; Michael J. Dillon; T. Martin Barratt

Publisher
Springer
Year
1989
Tongue
English
Weight
577 KB
Volume
3
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