421 top medical experts on Spinal Muscular Atrophies of Childhood across 28 countries and 27 U.S. states, including 296 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Spinal Muscular Atrophies of Childhood: A group of recessive inherited diseases that feature progressive muscular atrophy and hypotonia. They are classified as type I (Werdnig-Hoffman disease), type II (intermediate form), and type III (Kugelberg-Welander disease). Type I is fatal in infancy, type II has a late infantile onset and is associated with survival into the second or third decade. Type III has its onset in childhood, and is slowly progressive. (J Med Genet 1996 Apr:33(4):281-3)
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Nervous System Heredodegenerative Disorders (865), Spinal Muscular Atrophy (2,354).
  4. Clinical Trials ClinicalTrials.gov : at least 22 including 3 Active, 12 Completed, 2 Recruiting
  5. Synonyms: Infantile Spinal Muscular Atrophy,  Juvenile Spinal Muscular Atrophy,  Kugelberg-Welander Disease,  Infantile Spinal Muscular Atrophy,  Infantile Spinal Muscular Atrophy,  Juvenile Spinal Muscular Atrophy,  Werdnig-Hoffmann Disease


  

        

                    


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