oxaluria

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oxaluria

[‚äk·səl′yu̇r·ē·ə]
(medicine)
The presence of oxalic acid or oxalates in the urine.
References in periodicals archive ?
Testing for Oxf can become part of the routine metabolic evaluation of patients with hyperoxaluria and kidney stone disease.
formigenes, if taken orally with meals, will degrade oxalate throughout the GI-tract and reduce absorptive hyperoxaluria.
A New Method for Treatment of Hyperoxaluria and Kidney Stone Disease: Pyridoxamine Inhibits Kidney Crystal Formation in Hyperoxaluric Rats, S.
Unless one has hypercalciuria type II and hyperoxaluria (primary and enteric), there is no reason to avoid healthful foods that contain natural oxalates found in plants.
previously holds orphan drug designations in the EU and the US for the treatment of Primary Hyperoxaluria.
Description: This case study is a hemodialysis patient who had primary hyperoxaluria with associated kidney failure.
Late diagnosis of primary hyperoxaluria after failed kidney transplantation.
In children, the most common causes for CLKT are congenital diseases affecting both liver and kidney, such as primary hyperoxaluria type 1 (PH1) and autosomal recessive polycystic kidney disease (ARPKD).
While several metabolic disorders, such as primary hyperparathyroidism, hereditary cystinuria, and primary hyperoxaluria are known to cause nephrolithiasis, most stones are idiopathic in nature (3,8).
In 2006, the Chronicle reported how tests at the RVI and in Birmingham, confirmed Stephen thankfully did not have the rare and life-threatening primary hyperoxaluria, but still needed transplants from his parents to survive.
Primary hyperoxaluria is an inherited disorder of carbohydrate metabolism.