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Generalized tonic-clonic seizures as the initial symptom of late-onset Krabbe disease: a Case Report
CASE REPORT article Volume 19 - 2025 | https://doi.org/10.3389/fnbeh.2025.1564676 This article is part of the Research TopicGenotype-Phenotype Correlations, Genetic Mechanisms of Phenotypic Heterogeneity, Optimized Diagnosis and Targeted Therapies in Epilepsy and Neurodevelopmental DisordersView all articles Introduction Krabbe disease (KD) is an autosomal recessive leukodystrophy caused by mutations in the GALC gene, which encodes galactocerebrosidase.
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