29 top medical experts on Encephaloclastic Proliferative Vasculopathy across 4 countries. This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Encephaloclastic Proliferative Vasculopathy: A rare, genetic neurological disorder characterized by hydranencephaly, distinctive glomeruloid vasculopathy in the central nervous system and retina, polyhydramnios and fetal akinesia with arthrogryposis. The disorder is usually prenatally lethal. In rare reported cases that survived beyond infancy, severe intellectual and neurologic disability with seizures, microcephaly and absence of functional movements were reported.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Fowler Type Hydranencephaly,  Hydrocephaly-Hydranencephaly due to Cerebral Vasculopathy


  

        

                    


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