A case of primary hyperoxaluria developing end stage renal failure in infancy Son dönem böbrek yetmezliǧi gelişen bir primer hiperokzalüri olgusu

Akbalik M., Bek K., Karadeniz Ş., Özkaya O., Saǧ Taşdöven Ç., Baysal M. K.

Ondokuz Mayis Universitesi Tip Dergisi, vol.23, no.2, pp.65-68, 2006 (Scopus) identifier

  • Publication Type: Article / Article
  • Volume: 23 Issue: 2
  • Publication Date: 2006
  • Journal Name: Ondokuz Mayis Universitesi Tip Dergisi
  • Journal Indexes: Scopus
  • Page Numbers: pp.65-68
  • Keywords: Nephrocalcinosis, Primary hyperoxaluria, Renal failure
  • Ondokuz Mayıs University Affiliated: Yes

Abstract

Primary hyperoxaluria is a rare, autosomal recessive inherited disease which is characterísed by recurrent urolithiasis, nephrocalcinosis and oxalate deposition throughout the body. We present here 45 days old male infant with early onset nephrocalcinosis and end stage renal disease due to primary hyperoxaluria.