Literature DB >> 6703940

Monomelic amyotrophy.

M Gourie-Devi, T G Suresh, S K Shankar.   

Abstract

From 1977 through 1981, we examined 23 patients with single-limb atrophy. Thirteen had upper-limb and ten had lower-limb involvement. The characteristic clinical features were insidious onset in the second and third decades, male preponderance, sporadic occurrence, wasting and weakness confined to one limb, and absence of involvement of the cranial nerves, cerebrum, brain stem, and sensory system. The electromyographic features, along with histologic features of neurogenic atrophy, were suggestive of an anterior horn cell lesion. The slow progression of illness for two to four years followed by a stationary phase was observed. There was no clinical evidence of involvement of the other three limbs even in patients with long-standing illness of ten to 15 years' duration.

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Year:  1984        PMID: 6703940     DOI: 10.1001/archneur.1984.04050160050015

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


  24 in total

1.  Peripheral and segmental spinal abnormalities of median and ulnar somatosensory evoked potentials in Hirayama's disease.

Authors:  A Polo; M Curro' Dossi; A Fiaschi; G P Zanette; N Rizzuto
Journal:  J Neurol Neurosurg Psychiatry       Date:  2003-05       Impact factor: 10.154

2.  Benign monomelic amyotrophy: description of a patient with a focal motor neuron disorder.

Authors:  P Di Bella; F Logullo; D Tulli; M Ragno; M Scarpelli
Journal:  Ital J Neurol Sci       Date:  1992-02

3.  Hirayama disease: a frequently undiagnosed condition with simple inexpensive treatment.

Authors:  Rajesh Verma; Rakesh Lalla; Tushar B Patil; Arvind Gupta
Journal:  BMJ Case Rep       Date:  2012-12-06

4.  Madras pattern of motor neuron disease in South India.

Authors:  M Gourie-Devi; T G Suresh
Journal:  J Neurol Neurosurg Psychiatry       Date:  1988-06       Impact factor: 10.154

5.  Focal cervical poliopathy causing juvenile muscular atrophy of distal upper extremity: a pathological study.

Authors:  K Hirayama; M Tomonaga; K Kitano; T Yamada; S Kojima; K Arai
Journal:  J Neurol Neurosurg Psychiatry       Date:  1987-03       Impact factor: 10.154

6.  Juvenile muscular atrophy of distal upper extremities.

Authors:  C T Tan
Journal:  J Neurol Neurosurg Psychiatry       Date:  1985-03       Impact factor: 10.154

Review 7.  [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

8.  Lack of cervical paraspinal muscle involvement in juvenile distal spinal muscular atrophy: an electromyographic study on 15 cases.

Authors:  K P Kao; K P Lin; C M Chern; Z A Wu; C P Tsai; K K Liao
Journal:  J Neurol       Date:  1993-05       Impact factor: 4.849

9.  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

10.  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

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