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Brain Dev ; 37(3): 352-5, 2015 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-24852949

RESUMEN

Congenital bilateral perisylvian syndrome (CBPS) is a type of cortical developmental abnormality associated with distinctive clinical and imaging features. Clinical spectrum of this syndrome is quite heterogeneous, with different degrees of neurological impairment in affected individuals. High-definition magnetic resonance imaging (MRI) has a great importance in revealing the presence of CBPS, but is limited in elucidating the heterogeneous clinical spectrum. The arcuate fasciculus (AF) is a prominent language tract in the perisylvian region interconnecting Broca and Wernicke areas, and has a high probability of being affected developmentally in CBPS. Herein, we report a case of CBPS with investigation of AF using diffusion tensor imaging (DTI) and fiber tractography in relation to clinical findings. We postulated that proven absence of AF on DTI and fiber tractography would correlate with a severe phenotype of CBPS.


Asunto(s)
Anomalías Múltiples/diagnóstico , Imagen de Difusión Tensora , Discapacidad Intelectual/diagnóstico , Malformaciones del Desarrollo Cortical/diagnóstico , Anomalías Múltiples/patología , Anomalías Múltiples/fisiopatología , Adulto , Femenino , Humanos , Discapacidad Intelectual/patología , Discapacidad Intelectual/fisiopatología , Malformaciones del Desarrollo Cortical/patología , Malformaciones del Desarrollo Cortical/fisiopatología , Vías Nerviosas/anomalías
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