Late-onset globoid cell leukodystrophy
- 1 June 1990
- journal article
- research article
- Published by Springer Nature in Child's Nervous System
- Vol. 6 (4) , 194-197
- https://doi.org/10.1007/bf01850970
Abstract
During the past 12 years, ten cases of globoidcell leukodystrophy (GLD) have been followed up: seven of these patients were affected by the late infantile form. The authors point out the clinical aspects and the course of these patients and stress the high frequency of this form of GLD in Sicily.This publication has 5 references indexed in Scilit:
- Infantile and fetal globoid cell leukodystrophy: Analysis of galactosylceramide and galactosylsphingosineAnnals of Neurology, 1988
- Hydrolysis of galactosylceramide is catalyzed by two genetically distinct acid beta-galactosidases.Journal of Biological Chemistry, 1985
- Late-Onset Globoid Cell Leucodystrophy (Krabbe's Disease)Neuropediatrics, 1985
- Globoid cell leukodystrophy: Additional deficiency of psychosine galactosidaseBiochemical and Biophysical Research Communications, 1972