유전성 경직성 하반신마비 증례보고

• 영문명: A case Report of Hereditary Spastic paraparesis
• 발행기관: 대한임상노인의학회
• 저자명: 신준호(Joon Ho Shin) 김성우(Kim Sung Wu) 이규훈(Kyu Hoon Lee) 박시복(Si Bog Park)
• 간행물 정보: 『대한임상노인의학회지』대한임상노인의학회지 제4권 제4호, 57~62쪽, 전체 5쪽
• 주제분류: 의약학 > 기타의약학
• 파일형태: PDF
• 발행일자: 2003.12.30

영문 초록

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.

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키워드

Hereditary spastic paraparesis Toe gait