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신준호(Joon Ho Shin),김성우(Kim Sung Wu),이규훈(Kyu Hoon Lee),박시복(Si Bog Park) 대한임상노인의학회 2003 대한임상노인의학회지 Vol.4 No.4
Hereditary spastic paraparesis (HSP), or Strumpell-Lorrain syndrome, is a heterogenous group of hereditary neurodegenerative disorder of the central nervous system in which the primary clinical manifestation is a slowly progressive bilateral, spastic paraparesis. This paper is reporting a case of pure hereditary spastic paraparesis, which is the onset were 26 years ago. Physical examination revealed normoactive deep tendon reflexs in all four extremities with extensor plantar reflex and equinus. Electrodiagnostic study revealed no electrophysiological abnormality. The mode of inheritance of were autosomal dominant and were consistant those of type I of Harding's classification.