换一批
换一批摘要篇首： Primary hyperoxaluria (PH) is a rare autosomal recessive disorder of glyoxylate metabolism in which specific hepatic enzyme deficiencies result in overproduction of oxalate. Because oxalate is excreted exclusively by the kidney, hyperoxaluria leads to calcium oxalate nephrolithiasis, nephrocalcinosis, and renal failure.
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栏目名称
IMAGES FOR DIAGNOSIS
DOI
10.3760/cma.j.issn.0366-6999.2009.22.023
发布时间
2010-01-19
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