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- W2034785443 abstract "L’angiopathie amyloïde est la plus fréquente des microangiopathies cérébrales sans rapport direct avec l’hypertension artérielle. Ses liens avec la maladie d’Alzheimer en font une entité de définition complexe et de diagnostic difficile, d’autant que ses manifestations cliniques et radiologiques sont variées. D’autres microangiopathies cérébrales non liées à l’hypertension artérielle ont été décrites ces 20 dernières années avec l’avènement de l’IRM. La plupart d’entre elles sont d’origine génétique. La plus fréquente, cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), est une affection autosomique dominante dont les conséquences cliniques peuvent être majeures pour des sujets jeunes. D’autres formes génétiques, le plus souvent exceptionnelles, ont été rapportées récemment. Amyloid angiopathy is probably the most frequent non-hypertensive cerebral microangiopathy. Because of its close relationships with Alzheimer's disease, its definition and diagnosis may be difficult. Its clinical and radiological phenotype is quite variable. Other forms of non-hypertensive cerebral microangiopathies have been reported lately with the development of brain MRI. Most of them are of genetic origin. The most frequent, cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), is a monogenic disease with eventual devastating clinical consequences affecting young patients. Other forms, particularly of genetic origin, are regularly reported." @default.
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- W2034785443 date "2012-12-01" @default.
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- W2034785443 title "Partie 2 : angiopathie amyloïde cérébrale et formes génétiques de maladies des petites artères cérébrales" @default.
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- W2034785443 doi "https://doi.org/10.1016/j.praneu.2012.08.002" @default.
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