19 top medical experts on Jerash type Spinal muscular atrophy across 2 countries. This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Jerash type Spinal muscular atrophy: A rare, genetic, neuromuscular disease characterized by progressive, symmetrical, moderate to severe, distal muscle weakness and atrophy, without sensory involvement, first affecting the lower limbs (towards the end of the first decade) and then involving (within two years) the upper extremities. Patients typically develop foot drop, pes varus, hammer toes and claw hands. Pyramidal tract signs (such as brisk knee reflexes and positive Babinski sign) with absent ankle reflexes are initially associated but regress as disease stabilizes (~10 years after onset).
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Jerash type Hereditary motor neuropathy,  Jerash type distal Motor neuropathy,  Jerash Type Distal Hereditary Motor Neuronopathy,  Jerash type distal hereditary motor Neuropathy,  2 Autosomal Recessive Distal Spinal Muscular Atrophy


  

        

                    


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