265 top medical experts on Focal cortical dysplasia of Taylor across 35 countries and 17 U.S. states, including 96 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Focal cortical dysplasia of Taylor: Isolated focal cortical dysplasia is a rare, genetic, non-syndromic cerebral malformation due to abnormal neuronal migration disorder characterized by variable-sized, focalized malformations located in any part(s) of the cerebral cortex, which manifests with drug-resistant epilepsy (usually leading to intellectual disability) and behavioral disturbances. Abnormal MRI findings (e.g. abnormal white and/or grey matter signal, blurred gray-white matter junction, localized volume loss, cortical thickening, abnormal gyral pattern, abnormal hippocampus) and variable histopathologic patterns are associated.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Cortical Dysplasia of Taylor with Balloon Cells,  Cortical dysplasia of Taylor,  FCDT,  Type IIa Focal Cortical Dysplasia of Taylor,  Type IIb Focal Cortical Dysplasia of Taylor,  Type II Focal Cortical Dysplasia,  type 2 Focal cortical dysplasia


  

        

                    


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