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Autosomal recessive polycystic kidney disease in 15 Arab children

✍ Scribed by T. K. Mattoo; Y. Khatani; B. Ashraf

Publisher
Springer
Year
1994
Tongue
English
Weight
294 KB
Volume
8
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