Catalog

Autosomal dominant familial haematuria - retinal arteriolar tortuosity - contractures

No MMS code

Link to WHO Definition

Autosomal dominant familial haematuria - retinal arteriolar tortuosity - contractures – http://id.who.int/icd/entity/733821001

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.