Primary hyperoxaluria with development of renal failure during infancy: Report of two cases
Primary hyperoxaluria is a rare genetic disorder in glyoxylatemetabolism that leads to systemic overproductionof oxalate. The disorder results in overproduction andexcessive urinary excretion of oxalate, causing recurrenturolithiasis and nephrocalcinosis. As glomerular filtrationrate declines due to...
| Main Authors: | , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Dicle University Medical School
2012-12-01
|
| Series: | Dicle Medical Journal |
| Subjects: | |
| Online Access: | http://www.diclemedj.org/upload/sayi/4/Dicle%20Med%20J-01135.pdf |