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[营养不良性面肩肱综合征引发的诊断问题(作者译)]

[Diagnostic problems posed by hypotrophic facio-scapulo-humeral syndromes (author's transl)].

作者信息

Grassi E, Marbini A, Marchini C, Parma M, Zampollo A

出版信息

Ateneo Parmense Acta Biomed. 1976 Jan-Feb;47(1):95-101.

PMID:1016276
Abstract

The Authors, on the ground of the literature and of their own observations, stress the diagnostic non specificity of hypotrophic facio-scapulo-humeral syndromes: these sindromes, contrary to the current opinion, aren't always of primitive myodistrophic nature but may also be "neurogenic", inflammatory, collagenopathis, etc. In this connection they present an illustrative case of facio-scapulo-humeral syndrome which had clinical features typically "myogenic" but turned out to be "neurogenic" after electromyographic and histochemical investigation.

摘要

作者基于文献及自身观察结果,强调了萎缩性面肩肱型综合征的诊断非特异性:与目前观点相反,这些综合征并非总是原发性肌营养不良性的,也可能是“神经源性”、炎症性、胶原病性等。就此,他们展示了一个面肩肱型综合征的典型病例,该病例临床特征典型为“肌源性”,但经肌电图和组织化学检查后发现是“神经源性”。

相似文献

1
[Diagnostic problems posed by hypotrophic facio-scapulo-humeral syndromes (author's transl)].[营养不良性面肩肱综合征引发的诊断问题(作者译)]
Ateneo Parmense Acta Biomed. 1976 Jan-Feb;47(1):95-101.
2
[Neurogenic atrophy simulating facio-scapulo humaral dystrophy. On the facio-scapulo-humeral form of spibal atrophy in young adults].[模拟面肩肱型肌营养不良的神经源性萎缩。关于年轻人面肩肱型脊髓性肌萎缩]
Arch Neurobiol (Madr). 1974 Jan-Feb;37(1):11-30.
3
[Case of facio-scapulo-humeral muscular dystrophy with mitochondrial inclusion bodies found in muscle and liver biopsy].[在肌肉和肝脏活检中发现线粒体包涵体的面肩肱型肌营养不良病例]
Rinsho Shinkeigaku. 1976 Oct;16(10):706-14.
4
Facio-scapulo-humeral muscular dystrophy. Report of a case.
Indian J Pediatr. 1967 May;34(232):186-8. doi: 10.1007/BF02776967.
5
The differential diagnosis of the myogenic (facio)-scapulo-peroneal syndrome.肌源性(面)肩胛-腓骨综合征的鉴别诊断。
Eur Neurol. 1968;1(5):275-307. doi: 10.1159/000113669.
6
Facio-scapulo-humeral muscular dystrophy in a patient with one paretic leg due to poliomyelitis.一名因小儿麻痹症导致单腿麻痹的患者患面肩肱型肌营养不良症。
J Neurol Sci. 1970 Jan;10(1):1-10. doi: 10.1016/0022-510x(70)90087-0.
7
[Articulation disorder as the initial manifestation of facioscapulohumeral muscular dystrophy in childhood].
Klin Padiatr. 1986 Mar-Apr;198(2):119-21. doi: 10.1055/s-2008-1026865.
8
[Landouzy-Dejerine syndrome. Evolution of the concept of facio-scapulo-humeral amyotrophia].
Rev Neurol (Paris). 1977 Apr;133(4):279-82.
9
[Rapidly progressing facio-scapulo-humero-femoro-peroneal muscular dystrophy with sensorineural deafness].
Zh Nevropatol Psikhiatr Im S S Korsakova. 1991;91(9):5-8.
10
[A case of the facio-scapulo-humeral type of acute progressive muscular dystrophy with early beginning and acute course in a 9-year-old boy].[一名9岁男孩患面肩肱型急性进行性肌营养不良症,起病早且病程急]
Neurol Neurochir Pol. 1968 Jan-Feb;2(1):105-8.