Autosomal dominant familial haematuria - retinal arteriolar tortuosity - contractures (Q106650): Difference between revisions
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16 August 2026
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Latest revision as of 13:38, 17 August 2026
Autosomal dominant familial haematuria - retinal arteriolar tortuosity - contractures syndrome is characterised by the association of haematuria (without proteinuria) with extrarenal manifestations: retinal arterial tortuosities responsible for retinal haemorrhages, cardiac arrhythmia, Raynaud phenomena and congenital muscular contractures.
| Language | Label | Description | Also known as |
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| default for all languages | ID_733821001 |
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| English | Autosomal dominant familial haematuria - retinal arteriolar tortuosity - contractures |
Autosomal dominant familial haematuria - retinal arteriolar tortuosity - contractures syndrome is characterised by the association of haematuria (without proteinuria) with extrarenal manifestations: retinal arterial tortuosities responsible for retinal haemorrhages, cardiac arrhythmia, Raynaud phenomena and congenital muscular contractures. |
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CID11:ID_733821001
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dki-india-ID_733821001
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Concluído
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16 August 2026
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