Encephalopathy due to hydroxykynureninuria (Q89412): Difference between revisions
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13 August 2026
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Latest revision as of 16:06, 15 August 2026
Encephalopathy due to hydroxykynureninuria is characterised by psychomotor retardation and nonprogressive encephalopathy associated with urinary excretion of large amounts of kynurenine, 3-hydroxykynurenine, and xanthurenic acid. It has been described in less than 30 patients. Other manifestations may include muscular hypertonia, headaches and stereotyped gestures. This disorder is transmitted as an autosomal recessive trait. It is caused by a defect in kynureninase, an enzyme of the tryptophane catabolic pathway.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1145853843 |
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| English | Encephalopathy due to hydroxykynureninuria |
Encephalopathy due to hydroxykynureninuria is characterised by psychomotor retardation and nonprogressive encephalopathy associated with urinary excretion of large amounts of kynurenine, 3-hydroxykynurenine, and xanthurenic acid. It has been described in less than 30 patients. Other manifestations may include muscular hypertonia, headaches and stereotyped gestures. This disorder is transmitted as an autosomal recessive trait. It is caused by a defect in kynureninase, an enzyme of the tryptophane catabolic pathway. |
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CID11:ID_1145853843
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dki-india-ID_1145853843
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Concluído
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13 August 2026
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