Atypical clinical cases of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)


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Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a hereditary CNS disease with autosomal dominant inheritance caused by NOTCH3 gene mutations. In classic cases, CADASIL manifests with headaches, repeated cerebrovascular disorders, and progressive cognitive decline. Cerebral magnetic resonance imaging plays an important diagnostic role as it reveals multiple lacunar infarcts in the basal ganglia, brainstem, and cerebellum, as well as focal white matter lesions and diffuse leukoaraiosis changes. CADASIL can sometimes have other symptoms and be disguised as phenotypes atypical of this disease. We report two genetically confirmed cases of CADASIL with atypical clinical presentation that manifested with predominantly cerebellar or essential tremor combined with cognitive and affective disorders. The main principles of diagnosis of this disease characterized by clinical polymorphism are discussed.

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Anna Moroz

Research Center of Neurology

编辑信件的主要联系方式.
Email: snillario@gmail.com
俄罗斯联邦, Moscow

Natalia Abramycheva

Research Center of Neurology

Email: snillario@gmail.com
俄罗斯联邦, Moscow

Ekaterina Ivanova

Research Center of Neurology

Email: snillario@gmail.com
俄罗斯联邦, Moscow

Rodion Konovalov

Research Center of Neurology

Email: snillario@gmail.com
ORCID iD: 0000-0001-5539-245X

Cand. Sci. (Med.), senior researcher, Neuroradiology department

俄罗斯联邦, 125367 Moscow, Volokolamskoye shosse, 80

Sofiya Timerbaeva

Research Center of Neurology

Email: snillario@gmail.com
俄罗斯联邦, Moscow

Sergey Illarioshkin

Research Center of Neurology

Email: snillario@gmail.com
ORCID iD: 0000-0002-2704-6282

D. Sci. (Med.), Prof., Corr. Member of the Russian Academy of Sciences, Deputy Director, Head, Department for brain research

俄罗斯联邦, Moscow

参考

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版权所有 © Moroz A.A., Abramycheva N.A., Ivanova E.O., Konovalov R.N., Timerbaeva S.L., Illarioshkin S.N., 2017

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