Pathogenesis of leukodystrophy for Krabbe disease: Molecular mechanism and clinical treatment

被引:39
作者
Sakai, Norio [1 ]
机构
[1] Osaka Univ, Grad Sch Med, Dept Pediat, Suita, Osaka 5650871, Japan
关键词
Krabbe disease; Globoid-cell leukodystrophy; Hematopoietic stem cell transplantation; GLOBOID-CELL LEUKODYSTROPHY; HUMAN GALACTOCEREBROSIDASE; LATE-ONSET; MOUSE; CDNA; EXPRESSION; PHENOTYPE; MUTATION; TWITCHER; CLONING;
D O I
10.1016/j.braindev.2009.03.001
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We reported the basic concept of the pathology of leukodystrophy with emphasis on Krabbe disease. First, the normal process of myelination and the pathology of demyelination will be described, emphasizing the course inducing neuro-inflammation in its progression. After classifying metabolic leukodystrophy, the features of Krabbe disease (globoid-cell leukodystrophy) are explained as well as molecular cloning and mutation analysis of the galactocerebrosidase (GALC) gene. Finally, the experience of hematopoietic stem cell transplantation for patients with Krabbe disease is reported and the future possibility of therapy for the disease is summarized. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:485 / 487
页数:3
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