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Metachromatic leukodystrophy with late adult-onset: diagnostic clues and differences from other genetic leukoencephalopathies with dementia.

Authors :
Benzoni, Chiara
Moscatelli, Marco
Fenu, Silvia
Venerando, Anna
Salsano, Ettore
Source :
Journal of Neurology. May2021, Vol. 268 Issue 5, p1972-1976. 5p.
Publication Year :
2021

Abstract

In addition, common non-inherited forms of cerebral small vessel diseases [[6]], which can be associated with leukoencephalopathy and dementia, should be excluded based on lack of vascular risk factors and stroke events, and brain MRI features, including white matter lesion topography and absence of macro- and micro-hemorrhages. No microhemorrhage was present on T2*-weighted sequences (not shown) MLD is an autosomal recessive (AR) lysosomal disorder with typical onset in the first years of life. The original online version of this article was revised: The subtitle of the lower part of the table 1 is "Genetic leukoencephalopathies with dementia as predominant features" and not "Genetic leukoencephalopathies with dementia as prominent features". [Extracted from the article]

Details

Language :
English
ISSN :
03405354
Volume :
268
Issue :
5
Database :
Academic Search Index
Journal :
Journal of Neurology
Publication Type :
Academic Journal
Accession number :
149989259
Full Text :
https://doi.org/10.1007/s00415-020-10374-9