Xanthinuria type 1 (Q90423): Difference between revisions
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CID11:ID_1365934556 | |||||||||||||||
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dki-india-ID_1365934556 | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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13 August 2026
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Latest revision as of 17:23, 15 August 2026
Type I xanthinuria, a type of classical xanthinuria, is a rare autosomal recessive disorder of purine metabolism characterised by the isolated deficiency of xanthine dehydrogenase, causing hyperxanthinaemia with low or absent uric acid and xanthinuria, leading to urolithiasis, haematuria, renal colic and urinary tract infections, while some patients are asymptomatic and others suffer from kidney failure. Less common manifestations include arthropathy, myopathy and duodenal ulcer.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1365934556 |
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| English | Xanthinuria type 1 |
Type I xanthinuria, a type of classical xanthinuria, is a rare autosomal recessive disorder of purine metabolism characterised by the isolated deficiency of xanthine dehydrogenase, causing hyperxanthinaemia with low or absent uric acid and xanthinuria, leading to urolithiasis, haematuria, renal colic and urinary tract infections, while some patients are asymptomatic and others suffer from kidney failure. Less common manifestations include arthropathy, myopathy and duodenal ulcer. |
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CID11:ID_1365934556
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dki-india-ID_1365934556
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Concluído
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13 August 2026
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