Literature DB >> 26435801

Severe Spinal Injury in Hirayama Disease.

Cecilia Quarracino1, Florencia Aguirre1, Carlos A Rugilo2, Luciana De Negri1, Andrés M Villa1.   

Abstract

Hirayama disease is a rare neurological disorder characterized by an insidious progressive subacute unilateral or bilateral weakness of the hands and forearm muscles leading to a painless amyotrophy. The disease primarily affects young men in the second to third decades of life. It has always been described as a second motor neuron disease, thus sparing the pyramidal and sensitive pathways. It usually has a slow progression course of 3 to 5 years followed by stabilization. Since its initial description by Keyzo Hirayama in 1959, most cases have been reported in Asia, particularly Japan and India, although the disease reportedly has worldwide distribution.

Entities:  

Keywords:  Dynamic myelopathy; Hand atrophy; Hirayama disease; Oblique amyotrophy; Segmental spinal atrophy

Year:  2015        PMID: 26435801      PMCID: PMC4591454          DOI: 10.4184/asj.2015.9.5.794

Source DB:  PubMed          Journal:  Asian Spine J        ISSN: 1976-1902


  7 in total

1.  Magnetic resonance imaging in Hirayama disease.

Authors:  María Catalina Vargas; Mauricio Castillo
Journal:  J Radiol Case Rep       Date:  2011-03-01

2.  Electrophysiological features of Hirayama disease.

Authors:  Rong-Kuo Lyu; Ying-Chih Huang; Yih-Ru Wu; Hung-Chou Kuo; Long-Sun Ro; Chiung-Mei Chen; Hong-Shiu Chang
Journal:  Muscle Nerve       Date:  2011-08       Impact factor: 3.217

3.  Cervical spine MR imaging findings of patients with Hirayama disease in North America: a multisite study.

Authors:  V T Lehman; P H Luetmer; E J Sorenson; R E Carter; V Gupta; G P Fletcher; L S Hu; A L Kotsenas
Journal:  AJNR Am J Neuroradiol       Date:  2012-08-09       Impact factor: 3.825

4.  HyperIgEaemia in patients with juvenile muscular atrophy of the distal upper extremity (Hirayama disease).

Authors:  S Ito; S Kuwabara; T Fukutake; Y Tokumaru; T Hattori
Journal:  J Neurol Neurosurg Psychiatry       Date:  2005-01       Impact factor: 10.154

5.  A clinical study of Hirayama disease in Taiwan.

Authors:  Ying-Chih Huang; Long-Sun Ro; Hong-Shiu Chang; Chiung-Mei Chen; Yih-Ru Wu; Jian-Der Lee; Rong-Kuo Lyu
Journal:  Muscle Nerve       Date:  2008-05       Impact factor: 3.217

Review 6.  Nosology of juvenile muscular atrophy of distal upper extremity: from monomelic amyotrophy to Hirayama disease--Indian perspective.

Authors:  Kaukab Maqbool Hassan; Hirdesh Sahni
Journal:  Biomed Res Int       Date:  2013-08-26       Impact factor: 3.411

7.  Clinical and radiological profile of Hirayama disease: A flexion myelopathy due to tight cervical dural canal amenable to collar therapy.

Authors:  K M Hassan; Hirdesh Sahni; Atul Jha
Journal:  Ann Indian Acad Neurol       Date:  2012-04       Impact factor: 1.383

  7 in total

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