지원사업
학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
커뮤니티
연구자들이 자신의 연구와 전문성을 널리 알리고, 새로운 협력의 기회를 만들 수 있는 네트워킹 공간이에요.
논문 기본 정보
- 자료유형
- 학술저널
- 저자정보
- 발행연도
- 2021.12
- 수록면
- 71 - 75 (5page)
- DOI
- 10.18214/jend.2021.00052
이용수
초록· 키워드
오류제보하기
Progressive muscular atrophy (PMA) is a rare disease involving lower motor neuron degeneration.
Hypokalemic periodic paralysis (HypoPP) is a genetic disorder that causes temporary muscle paralysis due to decreased serum potassium levels. Mutations in the CACNA1S gene cause HypoPP. An altered locus closely linked near the CACNA1S gene suggests the possibility of motor neuron degeneration. However, PMA with HypoPP is very rare worldwide because HypoPP usually causes progressive muscle weakness involving a form of myopathy without motor neuron disease. In this report, we describe the case of a 64-year-old man who initially complained of weakness in only the left lower extremity, which subsequently progressed bilaterally. Hence, the patient was diagnosed with PMA with HypoPP based on serial electromyography and the presence of a CACNA1S mutation. Therefore, serial electromyography is necessary for middle-aged patients with progressive muscle weakness and a history of HypoPP.
목차
등록된 정보가 없습니다.
참고문헌 (10)
참고문헌 신청
Liewluck T / 2015 / Progressive muscular atrophy / Neurol Clin 33:761~773
Kim WK / 2009 / Study of 962 patients indicates progressive muscular atrophy is a form of ALS / Neurology 73:1686~1692
Ahlawat SK / 1999 / Hypokalaemic paralysis / Postgrad Med J 75:193~197
Pearson CM / 1964 / The periodic paralyses : differential features and pathological observations in permanent myopathic weakness / Brain 87:341~354
Links TP / 1994 / Familial hypokalemic periodic paralysis. Clinical, diagnostic and therapeutic aspects / J Neurol Sci 122:33~43
Kim WK / 2009 / Study of 962 patients indicates progressive muscular atrophy is a form of ALS / Neurology 73:1686~1692
Ahlawat SK / 1999 / Hypokalaemic paralysis / Postgrad Med J 75:193~197
Pearson CM / 1964 / The periodic paralyses : differential features and pathological observations in permanent myopathic weakness / Brain 87:341~354
Links TP / 1994 / Familial hypokalemic periodic paralysis. Clinical, diagnostic and therapeutic aspects / J Neurol Sci 122:33~43
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