203 top medical experts on Pontocerebellar Hypoplasia Type 1 across 17 countries and 5 U.S. states, including 25 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Pontocerebellar Hypoplasia Type 1: A severe, genetic form of pontocerebellar hypoplasia (PCH) characterized by spinal cord anterior horn cell degeneration in addition to pontocerebellar hypoplasia. Clinically, patients manifest with a severe global development deficit that is evident early on from difficulties in feeding and swallowing
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Support Organizations
  4. Synonyms: Pontocerebellar Hypoplasia With Anterior Horn Cell Disease,  Pontocerebellar Hypoplasia With Infantile Spinal Muscular Atrophy,  Type 1a Pontocerebellar Hypoplasia


  

        

                    


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