Adult-onset Krabbe disease presenting with progressive myoclonic epilepsy and asymmetric occipital lesions: A case report

Krabbe disease (KD), also known as globoid cell leukodystrophy, is a rare autosomal recessive condition caused by mutations in the galactocerebrosidase (GALC) gene. KD is more common in infants and young children than in adults. We reported the case of an adult-onset KD presenting with progressive m...

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Bibliographic Details
Main Authors: Yu Wang, Su-yue Wang, Kai Li, Yu-long Zhu, Kun Xia, Dan-dan Sun, Wen-long Ai, Xiao-ming Fu, Qun-rong Ye, Jun Li, Huai-zhen Chen
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-10-01
Series:Frontiers in Neurology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fneur.2022.1010150/full