88 top medical experts on Familial encephalopathy with neuroserpin inclusion bodies across 8 countries, including 4 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Familial encephalopathy with neuroserpin inclusion bodies: A rare serpinopathy characterized by progressive myoclonus epilepsy and/or pre-senile dementia with prominent frontal-lobe features and relative sparing of recall memory. In addition, other neurological manifestations like cerebellar symptoms and pyramidal signs may be present. Age of onset is variable, the disease having been reported in children as well as elderly patients. Neuropathological examination reveals the typical neuronal inclusions of mutated neuroserpin (Collins bodies).
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: With Neuroserpin Inclusion Bodies Familial Encephalopathy,  with Collins bodies familial Encephalopathy,  Familial Dementia with Neuroserpin Inclusion Bodies


  

        

                    


    Computing Expert Listing ...