Literature DB >> 9006413

Familial juvenile focal amyotrophy of the upper extremity (Hirayama disease). Superoxide dismutase 1 genotype and activity.

W Robberecht1, T Aguirre, L Van den Bosch, P Theys, H Nees, J J Cassiman, G Matthijs.   

Abstract

BACKGROUND: Juvenile focal amyotrophy of the arm is an unusual focal motor neuron disease that is rarely familial. Its pathogenesis is unknown. We recently described a family with amyotrophic lateral sclerosis associated with a mutation in the superoxide dismutase 1 (SOD1) gene substituting an aspartate for an alanine (D9OA). One of the carriers of this mutation had focal and nonprogressive amyotrophy of the arm, suggesting that focal amyotrophy might be associated with SOD1 mutations.
OBJECTIVES: To describe the phenotype of 2 brothers with juvenile focal amyotrophy of the upper extremity and to characterize their SOD1 genotype and SOD activity.
METHODS: Polymerase chain reaction and sequencing of the SOD1 gene and colorimetric measurement of the enzyme activity.
RESULTS: We compared the phenotype of our patients to that of 375 patients described in the Western literature. The 5 exons of the SOD1 gene were normal, as was the SOD activity in red blood cells.

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Year:  1997        PMID: 9006413     DOI: 10.1001/archneur.1997.00550130032012

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


  9 in total

1.  How does the neck flexion affect the cervical MRI features of Hirayama disease?

Authors:  Chao Hou; Hongbin Han; Xiaohong Yang; Xiaojuan Xu; Hui Gao; Dongsheng Fan; Yu Fu; Yu Sun; Bo Liu
Journal:  Neurol Sci       Date:  2012-01-03       Impact factor: 3.307

2.  Magnetic resonance imaging in Hirayama disease.

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

3.  A cervical myelopathy with a Hirayama disease-like phenotype.

Authors:  Chiara Cerami; Francesca Valentino; Federico Piccoli; Vincenzo La Bella
Journal:  Neurol Sci       Date:  2008-12-04       Impact factor: 3.307

Review 4.  [Hirayama disease in Germany: case reports and review of the literature].

Authors:  J-S Kang; S Jochem-Gawehn; H Laufs; A Ferbert; P Vieregge; U Ziemann
Journal:  Nervenarzt       Date:  2011-10       Impact factor: 1.214

5.  Hirayama disease is a pure spinal motor neuron disorder--a combined DTI and transcranial magnetic stimulation study.

Authors:  Kai Boelmans; Jörn Kaufmann; Sophie Schmelzer; Stefan Vielhaber; Malte Kornhuber; Alexander Münchau; Stephan Zierz; Charly Gaul
Journal:  J Neurol       Date:  2012-09-25       Impact factor: 4.849

6.  Mutational analysis of glycyl-tRNA synthetase (GARS) gene in Hirayama disease.

Authors:  Sergiu C Blumen; Vivian E Drory; Menachem Sadeh; Baruch El-Ad; Uri Soimu; Galina B Groozman; Jean-Pierre Bouchard; Lev G Goldfarb
Journal:  Amyotroph Lateral Scler       Date:  2010

7.  Benign monomelic amyotrophy with lower limb involvement in an adult: A case report.

Authors:  Taotao Hui; Zhi Bo Chang; Feng Han; Yongjun Rui
Journal:  Medicine (Baltimore)       Date:  2018-06       Impact factor: 1.889

Review 8.  Update on the Pathogenesis, Clinical Diagnosis, and Treatment of Hirayama Disease.

Authors:  Hongwei Wang; Ye Tian; Jianwei Wu; Sushan Luo; Chaojun Zheng; Chi Sun; Cong Nie; Xinlei Xia; Xiaosheng Ma; Feizhou Lyu; Jianyuan Jiang; Hongli Wang
Journal:  Front Neurol       Date:  2022-02-01       Impact factor: 4.003

9.  A Korean case of juvenile muscular atrophy of distal upper extremity (Hirayama disease) with dynamic cervical cord compression.

Authors:  Ohyun Kwon; Manho Kim; Kwang-Woo Lee
Journal:  J Korean Med Sci       Date:  2004-10       Impact factor: 2.153

  9 in total

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