Autosomal dominant familial haematuria - retinal arteriolar tortuosity - contractures (Q106650)

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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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ID_733821001
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    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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