Clinical features of Hirayama disease in mainland China

References

• Hirayama K, Toyokura Y, Tsubaki T. Juvenile muscular atrophy of unilateral upper extremity: a new clinical entity. Psychiatry Neurol Jpn. 1959; 61: 2190–8
   Google Scholar
• Hirayama K. Juvenile muscular atrophy of distal upper extremity (Hirayama disease). Int Med. 2000; 39: 283–90
   PubMed Web of Science ®Google Scholar
• Sobue I, Saito M, Iida M, Ando K. Juvenile type of distal and segmental muscular atrophy of upper extremities. Ann Neurol. 1978; 3: 429–32
   PubMed Web of Science ®Google Scholar
• Misra UK, Kalita J, Mishra VN, Kesari A, Mitta B. A clinical, magnetic resonance imaging, and survival motor neuron gene deletion study of Hirayama disease. Arch Neurol. 2005; 62: 120–3
   PubMedGoogle Scholar
• Misra UK, Kalita J. Central motor conduction in Hirayama disease. Electroencephalogr Clin Neurophysiol. 1995; 97: 73–6
   PubMedGoogle Scholar
• Gourie-Devi M, Nalini A. Long-term follow-up of 44 patients with brachial monomelic amyotrophy. Acta Neurol Scand. 2003; 107: 215–20
   PubMed Web of Science ®Google Scholar
• Peiris JB, Seneviratne KN, Wickremasinghe HR, Gunatilake SB, Gamage R. Non-familial juvenile distal spinal muscular atrophy of upper extremity. J Neurol Neurosurg Psychiatry. 1989; 52: 314–9
   PubMed Web of Science ®Google Scholar
• Kim JY, Lee KW, Roh JK, Chi JG, Lee SB. A clinical study of benign focal amyotrophy. J Korean Med Sci. 1994; 9: 145–54
   PubMedGoogle Scholar
• Tan CT. Juvenile muscular atrophy of distal upper extremities. J Neurol Neurosurg Psychiatry. 1985; 48: 285–6
   PubMed Web of Science ®Google Scholar
• Huang YC, Ro LS, Chang HS, Chen CM, Wu YR, Lee JD, et al. A clinical study of Hirayama disease in Taiwan. Muscle Nerve. 2008; 37: 576–82
   PubMed Web of Science ®Google Scholar
• Schroder R, Keller E, Flacke S, Schmidt S, Pohl C, Klockgether T, et al. MRI findings in Hirayama disease: flexion-induced cervical myelopathy or intrinsic motor neuron disease?. J Neurol. 1999; 246: 1069–74
   PubMed Web of Science ®Google Scholar
• Jeannet PY, Kuntzer T, Deonna T, Roulet-Perez E. Hirayama disease associated with a severe rhythmic movement disorder involving neck flexions. Neurology. 2005; 64: 1478–9
   PubMed Web of Science ®Google Scholar
• Visser M, Visser BWO, Verbeeten B. Electromyographic and computed tomographic findings in five patients with monomelic spinal muscular atrophy. Eur Neurol. 1988; 28: 135–8
   PubMed Web of Science ®Google Scholar
• Hirayama K, Tokumaru Y. Cervical dural sac and spinal cord in juvenile muscular atrophy of distal upper extremity. Neurol. 2000; 54: 1922–6
   PubMed Web of Science ®Google Scholar
• Zhang YD, Deng LK. Juvenile muscular atrophy of unilateral distal upper extremity (attached with reports of 10 cases). J Clinic Neurol. 1990; 3: 94–5
   Google Scholar
• Wang XH. A case of juvenile muscular atrophy of distal upper extremity. Chin Med J Metallurgical Industry. 1996; 13: 249
   Google Scholar
• Xie MY. Two cases of juvenile muscular atrophy distal upper extremity. Chin J of Practi Inter Med. 1997; 17: 682
   Google Scholar
• Li ZH, Zhang P, Chen Y, Zhao XL, Zhao XX, Deng RK. Clinical, electrophysiological and muscular pathology study of juvenile muscular atrophy of distal upper extremity. Chin J Neurol and Psych. 1994; 27: 131–4
   Google Scholar
• Yang XS, Xiao B, Zhang LF, Yang H, Liang JH. Juvenile muscular atrophy of unilateral distal upper extremity. Chin J Neurol and Psych. 2002; 28: 227–8
   Google Scholar
• Xu L, Huang BY, Li CY. Clinical and radiological analysis of four cases of Hirayama disease. Chin J Neurol and Psych. 2006; 32: 23–6
   Google Scholar
• Cao J, Fang Q, Dong WL. Two cases of juvenile muscular atrophy of distal upper extremity. Chin J Practi Inter Med. 2006; 22: 2111
   Google Scholar
• Wang XB. Right hand muscular atrophy for over one year: Hirayama disease (familial). Chin J Neurol and Psych. 2006; 32: 1–3
   Google Scholar
• Liu HJ, Li CY, He D, Chi C, Chui CX, Huang BY, et al. The value of MRI with neck flexed position in diagnosis of juvenile muscular atrophy of distal upper extremity. Chin J Radiol. 2006; 40: 745–7
   Google Scholar
• Gao HX, Zhong CY, Wang L, Tang YZ, Yang K. A case report on Hirayama disease misdiagnosis as motor neuron disease. Clin Misdiagnosis and Mistherapy. 2007; 20: 49–50
   Google Scholar
• Fu Y, Fan DS, Zhang J, Pei XL, Hai HB, Kang DX. Clinical features and cervical magnetic resonance imaging characteristics of Hirayama disease. J Peking Univer (Health Sciences) 2007; 39: 189–92
   Google Scholar
• Zhu D, Zhang JH, Chen JF, Feng JC. A case report of Hirayama disease (attached with electromyography change after 30 years of onset). J Neurol Disorders and Stroke. 2007; 24: 624–5
   Google Scholar
• Sun XT, Ma Y. A case of Hirayama disease. Modern J Integ Trad Chin Med West Med. 2007; 16: 3052–3
   Google Scholar
• Chen XY, Tang RH, Tang ZP, Lei HX. A case of Hirayama disease and literature review. Meta-Clinic. 2007; 22: 1256–7
   Google Scholar
• Wu YS. Analysis of misdiagnosis in four cases of Hirayama disease. Chin J Misdiag. 2007; 7: 3548–9
   Google Scholar
• Zhang YG, Wang YW, Liu ZS, Zheng JS. Analysis of a case of Hirayama disease misdiagnosed as cervical spondylotic myelopathy. Chin J Misdiagnosis. 2007; 7: 2049–50
   Google Scholar
• Xu JL, Geng LY, Liu YX, Chui AQ, Du CX. A case of Hirayama disease with symptom of muscular atrophy in the both upper limbs. Chin J Neurol. 2007; 40: 841
   Google Scholar
• Huang ZH. A case of Hirayama disease. Chin J Misdiagnosis. 2007; 7: 2676
   Google Scholar
• Dong ML, Liu J, Zhai M. Analysis of six cases of Hirayama disease. Chin J Misdiagnosis. 2008; 8: 973–4
   Google Scholar
• Wang WX, Gan MZ, Jiang Y, Zhang DZ, An XQ, Xu SX. Clinical analysis on a case of juvenile asymmetric muscular atrophy in the distal upper extremity. Chin J Pract Neurol Dis. 2008; 11: 88–90
   Google Scholar
• Li ZJ, Hu XQ, Tang N. Clinical neural electrophysiological characteristics of Hirayama disease. Neural Injury and Functional Reconstruction. 2008; 3: 422–5
   Google Scholar
• Liu L, Huang XS, Chen ZH, Liu SX, Pu CQ. Characteristics of electromyography and nerve conduction of Hirayama disease. Med J Chin People's Liber Army. 2008; 33: 88–90
   Google Scholar
• Kijima M, Hirayama K, Nakajima Y. Symptomatic and electrophysiological study on cold paresis in juvenile muscular atrophy of distal upper extremity (Hirayama disease). Rinsho Shinkeigaku. 2002; 42: 841–8
   PubMedGoogle Scholar
• Kao KP, Wu ZA, Chern CM. Juvenile lower cervical spinal muscular atrophy in Taiwan: report of 27 Chinese cases. Neuroepi. 1993; 12: 331–5
   PubMed Web of Science ®Google Scholar
• Hirayama K, Tomonaga M, Kitano K. The first autopsy case of ‘juvenile muscular atrophy of unilateral upper extremity’. Shinkei Naika (Neurol Med) 1985; 22: 85–8
   Google Scholar
• Hirabuki N, Mitomo M, Miura T, Hashimoto T, Kawai R, Kozuka T. Computed tomographic myelography characteristics of spinal cord atrophy in juvenile muscular atrophy of the upper extremity. Eur J Radiol. 1991; 13: 215–9
   PubMed Web of Science ®Google Scholar
• Mukai E, Matsuo T, Muto T, Takahashi A, Sobue I. Magnetic resonance imaging of juvenile-type distal and segmental muscular atrophy of upper extremities. Clin Neurol (Tokyo) 1987; 27: 99–107
   PubMedGoogle Scholar
• Pradhan S, Gupta RK. Magnetic resonance imaging in juvenile asymmetric segmental spinal muscular atrophy. J Neurol Sci. 1997; 146: 133–8
   PubMed Web of Science ®Google Scholar
• Normann D, Brant-Zawadzki M, Normann D. Magnetic resonance imaging of the central nervous system. Spine. 1987; 8: 289–328
   Google Scholar
• Araki K, Ueda Y, Michinaka C, Takamasu M, Takino T, Konishi H. An autopsy case of juvenile muscular atrophy of unilateral upper extremity (Hirayama disease). J Jpn Soc Intern Med. 1989; 78: 674–5
   PubMedGoogle Scholar
• Hirayama K. Juvenile muscular atrophy of distal upper extremity (Hirayama disease). Annual Review Neurology 1996, F Goto, K Takakura, M Kinoshita, N Yanagisawa, T Shimizu. Chugai-Igaku, Tokyo 1996; 249–60
   Google Scholar
• Tokumaru Y, Hirayama K. A cervical collar therapy for non-progressive juvenile spinal muscular atrophy of the distal upper limb (Hirayama disease). Rinsho Shinkeigaku (Clin Neurol) 1992; 32: 1102–6
   PubMedGoogle Scholar
• Chen CJ, Chen CM, Wu CL, Ro LS, Chen ST, Lee TH. Hirayama disease: MR diagnosis. AJNR Am J Neuroradiol. 1998; 19: 365–8
   PubMed Web of Science ®Google Scholar
• Tokumaru Y, Hirayama K. Cervical collar therapy for juvenile muscular atrophy of distal upper extremity (Hirayama disease): results from 38 cases. Rinsho Shinkeigaku. 2001; 41: 173–8
   PubMedGoogle Scholar
• Tashiro K, Kikuchi S, Itoyama Y, Tokumaru Y, Sobue G, Mukai E, et al. Nationwide survey of juvenile muscular atrophy of distal upper extremity (Hirayama disease) in Japan. Amyotrophic Lateral Sclerosis. 2006; 7: 38–45
   PubMed Web of Science ®Google Scholar
• Kohno M, Takahashi H, Ide K, Yamakawa K, Saitoh T, Inoue K. Surgical treatment for patients with cervical flexion myelopathy. J Neurosurg. 1999; 91: 33–42
   PubMed Web of Science ®Google Scholar
• Ogasa S, Taniguchi M, Maeda A. A case report of anterior spinal fusion for Hirayama disease. Seikei Geka. 1992; 43: 83–7
   Google Scholar
• Kono M, Takahashi H, Ishijima B, Inoue K. Surgical therapy in juvenile flexion myelopathy. Rinsho Shinkeigaku (Clin Neurol) 1996; 36: 278
   Google Scholar
• Konno S, Goto S, Murakami M, Mochizuki M, Motegi H, Moriya H. Juvenile amyotrophy of the distal upper extremity: pathological findings of the dura mater and surgical management. Spine. 1997; 22: 486–92
   PubMed Web of Science ®Google Scholar