115 top medical experts on autosomal dominant Spastic paraplegia 3 across 10 countries and 4 U.S. states, including 4 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. autosomal dominant Spastic paraplegia 3: A rare, pure or complex form of hereditary spastic paraplegia, with variable phenotype, typically characterized by childhood-onset of minimally progressive, bilateral, mainly symmetric lower limb spasticity and weakness, associated with pes cavus, scoliosis, sphincter disturbances and/or urinary bladder hyperactivity. Rare additional associated manifestations may include mild intellectual disability, axonal motor neuropathy, and seizures.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: 1 autosomal dominant Familial spastic paraplegia,  Fsp1 Familial spastic paraplegia 1,  SPG3A Spastic paraplegia 3a,  Spastic Paraplegia 3,  Spastic Paraplegia 3a,  Spastic Paraplegia Type 3a,  Spg3a,  Strumpell disease


  

        

                    


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