hyperoxaluria मीनिंग इन हिंदी

उदाहरण वाक्य

1. Type II hyperoxaluria is caused by mutations in this gene.
2. Primary hyperoxaluria is a rare autosomal recessive condition which usually presents in childhood.
3. Renal transplant is more effective and this is the primary treatment of severe hyperoxaluria.
4. Hyperoxaluria refers to oxalate derived from dietary sources or that which is secondary to malabsorption.
5. These include tumor lysis syndrome, acute phosphate nephropathy, and occasional cases of enteric hyperoxaluria.
6. One example is the hereditary disease primary hyperoxaluria, which causes kidney stones at an early age.
7. Primary hyperoxaluria is an autosomal recessive disease, meaning both copies of the gene contain the mutation.
8. This excess glyoxylate is then oxidized by lactate dehydrogenase to produce the oxalate that is characteristic of hyperoxaluria.
9. Hyperoxaluria that can potentially lead to oxalate nephropathy and irreversible renal failure is the most significant abnormality seen on urine chemistry studies.
10. "' Primary hyperoxaluria "'is a rare, inherited condition, resulting in increased excretion of oxalate, with oxalate stones being common.