The authors describe the principal forms of genetic leucodystrophies with unknown metabolic pathogenesis, indicating their main clinical signs and the new findings concerning the molecular genetic that are useful for the laboratory confirmation of the clinical suspicion.
This is a preview of subscription content, log in to check access.
Buy single article
Instant access to the full article PDF.
Price includes VAT for USA
Subscribe to journal
Immediate online access to all issues from 2019. Subscription will auto renew annually.
This is the net price. Taxes to be calculated in checkout.
About this article
Cite this article
Federico, A., Rufa, A., Battisti, C. et al. Genetic leukoencephalopathies with unknown metabolic pathogenesis. Neurol Sci 22, S108–S112 (2001). https://doi.org/10.1007/s100720100046
- Key words Leukodystrophies
- White matter disorders
- Neurodegenerative diseases