Clinical and neuroradiological findings
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Barone, R.; BrΓΌhl, K.; Stoeter, P.; Fiumara, A.; Pavone, L.; Beck, M.
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Article
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1996
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John Wiley and Sons
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English
β 64 KB
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In the present study the clinical course and imaging of early and late-onset forms of Krabbe disease are analyzed. We report on 11 patients with a biochemical diagnosis of galactosyl ceramide P-galactoside deficiency. T w o presented as the classic infantile form and died within the second year of l