oxalosis
(ok″să-lō′sĭs)

[oxalo- + -sis]
An autosomal recessive hereditary disease due to faulty metabolism of glyoxylic acid. Oxalic acid is elevated in the urine because of its increased production. Calcium oxalate can be deposited in body tissues, esp. in the kidneys.
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Citation
Venes, Donald, editor. "Oxalosis." Taber's Medical Dictionary, 25th ed., F.A. Davis Company, 2025. Nursing Central, nursing.unboundmedicine.com/nursingcentral/view/Tabers-Dictionary/737592/all/systemic_oxalosis.
Oxalosis. In: Venes DD, ed. Taber's Medical Dictionary. F.A. Davis Company; 2025. https://nursing.unboundmedicine.com/nursingcentral/view/Tabers-Dictionary/737592/all/systemic_oxalosis. Accessed April 6, 2025.
Oxalosis. (2025). In Venes, D. (Ed.), Taber's Medical Dictionary (25th ed.). F.A. Davis Company. https://nursing.unboundmedicine.com/nursingcentral/view/Tabers-Dictionary/737592/all/systemic_oxalosis
Oxalosis [Internet]. In: Venes DD, editors. Taber's Medical Dictionary. F.A. Davis Company; 2025. [cited 2025 April 06]. Available from: https://nursing.unboundmedicine.com/nursingcentral/view/Tabers-Dictionary/737592/all/systemic_oxalosis.
* Article titles in AMA citation format should be in sentence-case
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