Author/Authors :
Mamizadeh, Nahid Department of Pediatric Nephrology - Ali-Asghar Children hospital, Iran University of Medical Sciences , Hooman, Nakysa , Otukesh, Hasan , Hosieni, Rozita , Nickavar, Azar , Goldasteh, Mahya
Abstract :
Primary hyperoxaluria (PH) is a rare autosomal recessive disorder associated with defects in glyoxylate metabolism and overproduction of oxalate. Then, calcium oxalate is deposited in many organs such as the kidney
Keywords :
Clinical Features , Outcome in Children , Primary Hyperoxaluria , Single Center Experience
