伴有胼胝体变薄的遗传性痉挛性截瘫 - Suppr

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超能文献

Hereditary spastic paraplegia with thin corpus callosum.

作者信息

Raina Sujeet, Mokta Jitender K, Sharma Sanjiv

机构信息

Department of Medicine, Indira Gandhi Medical College, Shimla, Himachal Pradesh - 171 001, India.

出版信息

Ann Indian Acad Neurol. 2009 Jan;12(1):56-7. doi: 10.4103/0972-2327.48863.

DOI:10.4103/0972-2327.48863

PMID:20151015

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2811984/

Abstract

摘要

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Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration.SPG11基因的突变在伴有胼胝体变薄、认知功能减退和下运动神经元变性的常染色体隐性遗传性痉挛性截瘫中很常见。

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