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| Case Report | |||||
| Dementia and Neurocognitive Disorders 2014: 13: 1: 16-19 | |||||
| 기억장애가 유일한 임상양상으로 확인된 척수소뇌실조 2형 1예 | |||||
|---|---|---|---|---|---|
| 주재정, 한상우, 하상원, 한정호, 김두응, 양영순 | |||||
| 보훈공단 중앙보훈병원 신경과 | |||||
| Spinocerebellar Ataxia Type 2 with Only Clinical Feature of Memory Impairment: Case Report | |||||
| JaeJeong Joo, M.D., Sang Wo Han, M.D., Sang Won Ha, M.D., Jeong Ho Han, M.D., Doo Eung Kim, M.D., YoungSoon Yang, M.D. | |||||
| Department of Neurology, SVH Medical Center, Seoul, Korea | |||||
| Spinocerebellar ataxia (SCA) is one of a group of genetic disorders characterized by slowly progressive in-coordination of gait and often associated with poor coordination of hands, speech, and eye movements. There are more than 35 different types of spinocerebellar ataxias, each caused by a different genetic mutation. Spinocerebellar ataxia type 2 (SCA2) is a subtype of type I autosomal dominant cerebellar ataxia (ADCA type I) characterized by truncal ataxia, dysarthria, slowed saccades and less commonly ophthalmoparesis and chorea. The age at onset varies from 3 to 79 years (mean 33). Usually, the first symptom of the disease is the gait ataxia, followed by the cerebellar dysarthria. Of late, other clinical manifestations of SCA2 are the cognitive dysfunctions, which include frontal executive impairment, verbal short-term memory deficits as well as reduction of attention and concentration. We report a 56-year old woman identified as spinocerebellar ataxia type 2 (SCA2) with only clinical feature of memory impairment. | |||||
| Key Words: Spinocerebellar ataxia type 2, Memory impairment | |||||
| 대한치매학회지 (Dementia and Neurocognitive Disorders) |
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