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Thinning of the Corpus Callosum and Cerebellar Atrophy is Correlated with Phenotypic Severity in a Family with Spastic Paraplegia Type 11
BACKGROUND: Mutations in the spatacsin gene are associated with spastic paraplegia type 11 (SPG11), which is the most-common cause of autosomal recessive hereditary spastic paraplegia. Although SPG11 has diverse phenotypes, thinning of the corpus callosum is an important feature. CASE REPORT: Clinic...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Korean Neurological Association
2011
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3131536/ https://ncbi.nlm.nih.gov/pubmed/21779300 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3988/jcn.2011.7.2.102 |
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