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
- 2016.1
- 수록면
- 1,664 - 1,667 (4page)
이용수
초록· 키워드
오류제보하기
Hirayama disease is a slowly progressing benign motor neuron disease that affects the distal upper limb. A 29-year-old man visited the hospital with a 1-year history of weakened left proximal upper limb. He was diagnosed with Hirayama disease 9 years ago, while there was no further progression of the muscle weakness afterward. Atrophy and weakness was detected in proximal upper limb muscles. Magnetic resonance imaging and somatosensory evoked potentials were normal. Needle electromyography showed abnormal findings in proximal upper limb muscles. Our patient had Hirayama disease involving the proximal portion through secondary progression. Clinical manifestation and accurate electromyography may be useful for diagnosis. Rare cases with progression patterns as described here are helpful and have clinical meaning for clinicians.
목차
등록된 정보가 없습니다.
참고문헌 (13)
참고문헌 신청
Hirayama K / 2000 / Juvenile muscular atrophy of distal upper extremity(Hirayama disease) / Intern Med 39:283~290
Huang YL / 2011 / Hirayama disease / Neuroimaging Clin N Am 21:939~950
Lim YM / 2012 / Exome sequencing identifies KIAA1377 and C5orf42 as susceptibility genes for monomelic amyotrophy / Neuromuscul Disord 22:394~400
Tashiro K / 2006 / Nationwide survey of juvenile muscular atrophy of distal upper extremity(Hirayama disease)in Japan / Amyotroph Lateral Scler 7:38~45
Gourie-Devi M / 2003 / Long-term follow-up of 44 patients with brachial monomelic amyotrophy / Acta Neurol Scand 107:215~220
Huang YL / 2011 / Hirayama disease / Neuroimaging Clin N Am 21:939~950
Lim YM / 2012 / Exome sequencing identifies KIAA1377 and C5orf42 as susceptibility genes for monomelic amyotrophy / Neuromuscul Disord 22:394~400
Tashiro K / 2006 / Nationwide survey of juvenile muscular atrophy of distal upper extremity(Hirayama disease)in Japan / Amyotroph Lateral Scler 7:38~45
Gourie-Devi M / 2003 / Long-term follow-up of 44 patients with brachial monomelic amyotrophy / Acta Neurol Scand 107:215~220
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