What is Spastic paraplegia 3, autosomal dominant?
Main name of condition: Spastic paraplegia 3, autosomal dominant Other names or spellings for Spastic paraplegia 3, autosomal dominant: SPGA3, Strumpell disease, familial spastic paraplegia autosomal dominant, 1, FSP1, SPG3A, SPG3 FSP1, Familial spastic paraplegia, autosomal dominant, 1, SPG3, SPG3A, Strumpell disease Source – Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)