Pastores G M
Department of Neurology, New York University School of Medicine, New York, NY 10016, USA.
Int J Clin Pharmacol Ther. 2009;47 Suppl 1:S75-81. doi: 10.5414/cpp47075.
Krabbe disease (globoid cell leukodystrophy) is a neurodegenerative disorder that is caused by deficiency of the lysosomal enzyme galactosylceramidase. The resulting accumulation of incompletely metabolized galactocerebroside, which is a component of myelin, leads to progressive white matter disease. The severity of signs and symptoms is partly influenced by the causal mutations and corresponding residual enzyme activity. This review explains how the disease might manifest and discusses methods for diagnosis and staging of the disease process. The current understanding of the mechanisms underlying Krabbe disease is summarized, and therapeutic options--including current and investigational approaches--are outlined.
克拉伯病(球形细胞脑白质营养不良)是一种神经退行性疾病,由溶酶体酶半乳糖神经酰胺酶缺乏引起。髓鞘成分之一的半乳糖脑苷脂代谢不完全而蓄积,导致进行性白质疾病。体征和症状的严重程度部分受致病突变和相应残余酶活性的影响。本综述解释了该疾病可能的表现形式,并讨论了疾病进程的诊断和分期方法。总结了目前对克拉伯病潜在机制的认识,并概述了治疗选择,包括现有方法和研究中的方法。