Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8276458 | Journal of the Neurological Sciences | 2014 | 13 Pages |
Abstract
Several genetic diseases may be suspected in patients with middle or old age and white matter abnormalities. In only few instances, pathognomonic clinical or associated neuroimaging features help identifying a specific disease. Therefore, a comprehensive knowledge of the characteristics of these inherited white matter diseases appears important to improve the diagnostic work-up, optimize the choice of genetic tests, increase the number of diagnosed patients, and stimulate the research interest in this field.
Keywords
Familial amyloidosis of Finnish typeHCHWA-Dfragile X-associated tremor/ataxia syndromeFBDCARASILSVDADLDMERRFTIACADASILMELASFAFFXTAScerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathyFLAIRMRIfluid-attenuated inversion recoveryAdulthoodinheritedSmall vessel diseaseWhite matter diseaseMagnetic resonance imagingtransient ischemic attackFamilial British dementiaPhenotypeLeukoencephalopathyGenotype
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Authors
Serena Nannucci, Ida Donnini, Leonardo Pantoni,