%0 Journal Article
%T Systemic Oxalosis in Infants: Two Cases and Literature Review
%A G¨¹nd¨¹z
%A Z¨¹beyde
%A Ba£¿tu£¿
%A Funda
%A T¨¹lpar
%A Sebahat
%A Poyrazo£¿lu
%A Hakan
%J The Turkish Nephrology, Dialysis and Transplantation Journal
%D 2013
%I Turkish Society of Nephrology
%R 10.5262/tndt.2013.1002.13
%X The infantile form of primary hyperoxaluria is a very rare disease and often presents as a lifethreatening condition because of rapid progression to end-stage renal disease and systemic oxalosis. We described two infants with primary hyperoxaluria type 1 (PH1). Persistent severe hyponatremia and hypoalbuminemia were noted in both patients and cerebral and pulmonary involvements of systemic oxalosis were suspected in one patient. Such a severe phenotype of infantile PH1 is an important   nding that should be added to the list of manifestations of PH1.
%K Systemic oxalosis
%K Infant
%K Persistent hyponatremia and hypoalbuminemia
%K Pulmonary involvement
%U http://tndt.org/pdf/pdf_TNDT_934.pdf