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Frontal Aslant Tract Abnormality on Diffusion Tensor Imaging in an Aphasic Patient with 49, XXXXY Syndrome
BACKGROUND: 49, XXXXY is one of the most severe forms of chromosome aneuploidy and is characterized by developmental delay and profound language impairment; particularly involving expressive language functions. We describe the neurocognitive profile and structural anatomy of language pathway in a 2...
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| Publicado en: | Pediatr Neurol |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2015
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4747816/ https://ncbi.nlm.nih.gov/pubmed/26706051 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.pediatrneurol.2015.10.020 |
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