4 top medical experts on Autosomal Dominant Proximal Childhood Spinal Muscular Atrophy across 0 countries, including 1 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Autosomal Dominant Proximal Childhood Spinal Muscular Atrophy: A rare genetic neuromuscular disease characterized by early onset muscular weakness with predominant proximal lower limb involvement. The disorder is static or only mildly progressive. The severity of manifestations ranges from lethal, congenital muscular atrophy with arthrogryposis to asymptomatic with subclinical features.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Autosomal Dominant Kugelberg-Welander Syndrome,  Autosomal Dominant Proximal Juvenile Spinal Muscular Atrophy


  

        

                    


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