Abnormalities of developing white matter in lysosomal storage diseases

被引:37
作者
Folkerth, RD
机构
[1] Brigham & Womens Hosp, Dept Pathol Neuropathol, Boston, MA 02115 USA
[2] Harvard Univ, Childrens Hosp, Sch Med, Boston, MA 02115 USA
关键词
autopsy; brain development; dysmyelinogenesis; lysosomal storage disease; myelination; oligodendroglia;
D O I
10.1097/00005072-199909000-00001
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Inborn metabolic errors causing, lysosomal storage-have well-recognized effects on neuronal function and morphology. In some classically "neuronal" storage diseases, however neuroradiologic observations of infants have suggested a delay in central nervous system myelination based on persistently "immature" signal intensities monitored over time. This review summarizes reported neuropathologic evaluations of central white matter in infantile and juvenile patients and in corresponding animal models with lysosomal storage disorders. The observed neuropathology is examined in light of published studies of the biochemistry and microscopic anatomy of normal myelinogenesis. Finally, arguments are advanced that at least part of the deficiency of white matter is attributable to direct effects of the metabolic state on oligodendrocyte maturation and function, in addition to secondary effects on neurons and their axons.
引用
收藏
页码:887 / 902
页数:16
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