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Hereditary Spastic Paraplegia:     more detail

The Official Patient's Sourcebook on Hereditary Spastic Paraplegia: A Revised and Updated Directory for the Internet Age by Icon Health Publications, 2002-09 Hereditary spastic paraplegia: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Chitra, MBBS, MD Venkatasubramanian, 2005 Hereditary spastic paraplegia: An entry from Thomson Gale's <i>Gale Encyclopedia of Neurological Disorders</i> by Sandra Galeotti, 2005 On hereditary ataxia and spastic paraplegia (The treasury of human inheritance) by Julia Bell, 1939

lists with details

101. Log In Problems
     hereditary spastic Paraparesis (paraplegia). A group of disorders characterizedby progressive lower extremity weakness and spasticity.  
     http://www.medscape.com/pages/sites/dnas/glossary/ms

102. FSP Syndromes
     hereditary sensory neuropathy with spastic paraparesis (Cavanagh s variant) SPG21 spastic paraplegia with dementia extrapyramidal signs (Mast  
     http://www.neuro.wustl.edu/neuromuscular/spinal/fsp.html

103. 600363 SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT; SPG6
     Harding, AE hereditary pure spastic paraplegia a clinical and genetic studyof 22 families. J. Neurol. Neurosurg. Psychiat. 44 871883, 1981.  
     http://srs.sanger.ac.uk/srsbin/cgi-bin/wgetz?[omim-ID:600363] -e

104. The FSP Support Group - Home
     For people suffering from Familial spastic paraplegia. Includes a newsletter,discussion forum, links, and contact details.  
     http://www.fspgroup.org/
     
     Extractions: Welcome to the FSP Support Group The FSP Support Group is a 'self-help' group that aims to provide assistance to those suffering from Familial Spastic Paraplegia (also known as Hereditary Spastic Paraplegia or HSP). Members of the Group come primarily from the UK although we are expanding our frontiers with some international members from Ireland, Germany and France. We also have a number of professional associates. Members of the Group gain many benefits such as: The FSP Support Group was started in 1989 by Stephanie Wyatt to support her affected husband and son. Our membership is now nationwide and continues to rise. The aims of the group are to encourage and support sufferers. In addition, affected families are encouraged to support a genetic research programme by completing a family history tree chart. This pool of information is vital in identifying the source and origin of the condition with the view to reducing its occurrence. The current group awareness programme will hasten the work carried out by the team based at The National Hospital in London.

105. Hspinfo.org
     HSPINFO.ORG.  
     http://hspinfo.org/

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