(Strumpell-Lorrain Familial Spasmodic Paraplegia, Strumpell's Familial Paraplegia, Spasmodic Infantile Paraplegia, Spastic Congenital Paraplegia, Spastic Spinal Familial Paralysis)

Spastic Paraplegia Foundation, Inc. (SPF)

FSP (Familial Spastic Paraplegia) Support Group

Also See:

• Hereditary Spastic Paraplegia Overview, GeneReviews
• Hereditary Spastic Paraplegia, National Institute of Neurological Disorders and Stroke (NINDS)
• Hereditary Spastic Paraplegia, Neurology Department, University of Michigan, Ann Arbor
• Hereditary Spastic Paraplegia, About.com
• Hereditary Spastic Paraplegia, eMedicine, Nam-Jong Paik
• Hereditary Spastic Paraplegia, Google directory
• Online Mendelian Inheritance in Man
  • Kallmann Syndrome with Spastic Paraplegia, OMIM
  • Spastic Paraplegia 2, X-Linked; SPG2, OMIM, OMIM
  • Spastic Paraplegia 3, Autosomal Dominant; SPG3A, OMIM
  • Spastic Paraplegia 4, Autosomal Dominant, SPG4, OMIM
    
  • Spastic Paraplegia 15, Automal Recessive; SPG15, OMIM
  • Spastic Paraplegia 17; SPG17, OMIM
  • Spastic Paraplegia with Myoclonic Epilepsy, OMIM
  • Spastic Paresis, glacoma, and mental retardation, OMIM
  • Spastic Paraplegia with associated extraparamidal signs, OMIM
  • Spastic Quadriplegia, retinitis pigmentosa, and mental retardation, OMIM
  • Spastic Paraplegia with Neuropathy and Poikiloderma, OMIM
  • Spastic Paraplegia, Optic Atrophy, and Dementia, OMIM
• spastic paraplegia (SP), Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes, National Library Mecicine

• National organizations information on genetic conditions or birth defects
• Information for Siblings and Family Members

To locate a genetic counselor or clinical geneticist in your area:

• Professional Genetics Societies
• Genetic clinics, centers, departments

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