Article

Mild Cognitive Impairment in novel SPG11 Mutation-Related Sporadic Hereditary Spastic Paraplegia with Thin Corpus Callosum

2020-09-17

Abstract excerpt

<title>Abstract</title> <p><bold>Background: </bold><italic>SPG11 </italic>mutation-related autosomal recessive hereditary spastic paraplegia with thin corpus callosum (HSP-TCC) is the most common cause in complicated forms of HSP, usually presenting comprehensive mental retardation on early-onset stage preceding spastic paraplegias in childhood. However, there are still lots of sporadic late-onset HSP-TCC cases...

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Literature Corpus work: c4cf08ed-1ad6-5e3d-aa96-f41112830547
DOI: 10.21203/rs.3.rs-60928/v1

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