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27 Possible Causes for Xanthine Urolithiasis

  • Xanthinuria

    In a patient with xanthine urolithiasis secondary to hereditary xanthinuria (xanthine oxidase deficiency), allopurinol administration resulted in a 20 per cent increase in[ncbi.nlm.nih.gov] The analysis of its pedigree has shown that : a) the mode of transmission of xanthinuria is autosomal recessive; b) the occurence of xanthine urolithiasis is likely to be[ncbi.nlm.nih.gov] In about half of patients, ultrasonography reveals the presence of xanthine urolithiasis.[orpha.net]

  • Nephrolithiasis

    Xanthine stones form in patients with severe hyperuricemia taking allopurinol, or in those with the rare inherited forms of xanthinuria, while 2,8-dihydroxyadenine urolithiasis[ncbi.nlm.nih.gov]

  • Urolithiasis

    People afflicted with xanthinuria often produce stones composed of xanthine.[en.wikipedia.org] Urolithiasis has also been noted to occur in the setting of therapeutic drug use, with crystals of drug forming within the renal tract in some people currently being treated[en.wikipedia.org]

  • Xanthinuria Type 1

    Xanthine urolithiasis.[sjkdt.org] In about half of patients, ultrasonography reveals the presence of xanthine urolithiasis.[orpha.net] Pais VM, Lowe G, Lallas CD et al: Xanthine urolithiasis. Urology 2006, 67 (5), 1084.e9-11.[urologiapolska.pl]

  • Urate Kidney Stone

    .: Xanthine urolithiasis . Urology 2006, 67: 1084–2011.[link.springer.com] Treatment of uric acid urolithiasis with allopurinol: a xanthine oxidase inhibitor. J Urol 1967;97:340. 24. Türk C, Neisius A, Petrik A, et al. Urolithiasis.[jeleu.com]

  • Molybdenum Cofactor Deficiency Complementation Group B

    […] features of neonatal seizures, profound neurological abnormalities, abnormal facial features, ectopia lentis, urolithiasis and characteristic biochemical defects.[docslide.com.br] The molybdenum cofactor is essential for the function of three enzymes: sulphite oxidase, xanthine dehydrogenase and aldehyde oxidase; its deficiency leads to the typical[docslide.com.br]

  • Fabry Disease

    J Med Genet 33 : 682 –688, 1996 Pais VM Jr, Lowe G, Lallas CD, Preminger GM, Assimos DG: Xanthine urolithiasis.[jasn.asnjournals.org] These boys and others who are treated with allopurinal for a long time may also develop xanthinuria and xanthine urolithiasis with staghorn calculi. 16 On the other hand,[jasn.asnjournals.org]

  • Hereditary Hyperekplexia

    […] crystal nephropathy, urolithiasis, or renal failure.[emedicine.medscape.com] Deficiency of xanthine dehydrogenase results in plasma accumulation and excess urinary excretion of the highly insoluble xanthine, which may lead to arthropathy, myopathy,[emedicine.medscape.com] Xanthine continues to accumulate, despite the recycling of hypoxanthine, because of the metabolism of guanine to xanthine by the enzyme guanase (see image below).[emedicine.medscape.com]

  • Severe X-Linked Intellectual Disability Type Gustavson

    […] monosomy Xq28 X chromosome, trisomy Xp3 X chromosome, trisomy Xpter Xq13 X chromosome, trisomy Xq X chromosome, trisomy Xq25 X fragile site folic acid type Xa-Xk Xanthic urolithiasis[wikidoc.org] Xq28 X chromosome, trisomy Xp3 X chromosome, trisomy Xpter Xq13 X chromosome, trisomy Xq X chromosome, trisomy Xq25 X fragile site folic acid type Xa–Xk [ edit ] Xanthic urolithiasis[en.wikipedia.org] Xanthic urolithiasis[?] Xanthine oxydase deficiency[?] Xanthinuria[?] Xanthomatosis cerebrotendinous[?] Xanthophobia[?] Xenoglossophobia[?][encyclopedia.kids.net.au]

  • Xanthine Urolithiasis

    This may be effectively prevented by administration of allopurinol; however, its overdosage may result in xanthinuria and xanthine urolithiasis.[ncbi.nlm.nih.gov] We report here two children with xanthine urolithiasis.[ncbi.nlm.nih.gov] Xanthine urolithiasis.[sjkdt.org]

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