[诊断影像（29）。成人型近端脊髓性肌萎缩症]
[Diagnostic image (29). Adult form of proximal spinal muscular atrophy].
作者信息
Bronner I M, Linssen W H, de Visser M
机构信息
Sint Lucas Andreas Ziekenhuis, afd. Neurologie, Amsterdam.
出版信息
Ned Tijdschr Geneeskd. 2001 Mar 17;145(11):530.
PMID:11284287
Abstract
A 58-year-old man developed slowly progressive weakness of both legs due to the adult form of proximal spinal muscular atrophy.
摘要
一名58岁男性因成人型近端脊髓性肌萎缩症出现双下肢缓慢进行性无力。
相似文献
1
[Diagnostic image (29). Adult form of proximal spinal muscular atrophy].
Ned Tijdschr Geneeskd. 2001 Mar 17;145(11):530.
2
[Diagnostic difficulties in spinal muscular atrophy].
Arq Neuropsiquiatr. 2005 Mar;63(1):145-9. doi: 10.1590/s0004-282x2005000100026. Epub 2005 Apr 13.
3
Limb-girdle muscular dystrophy or spinal muscular atrophy: a source of diagnostic confusion?
J Med Genet. 1997 Nov;34(11):958-9. doi: 10.1136/jmg.34.11.958-a.
4
Rapid SMN1 deletion test using DHPLC to screen patients with spinal muscular atrophy.
Am J Med Genet. 2002 Nov 22;113(2):225-6. doi: 10.1002/ajmg.10744.
5
SMN2 deletion in childhood-onset spinal muscular atrophy.
Am J Med Genet. 2002 May 1;109(3):246; author reply 247. doi: 10.1002/ajmg.10354.
6
Comment on SMN2 deletion in childhood-onset spinal muscular atrophy.
Am J Med Genet. 2002 May 1;109(3):243-4; author reply 245. doi: 10.1002/ajmg.10277.
7
[Detection of SMN gene deletions in spinal muscular atrophy].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 1998 Apr 10;15(2):95-7.
8
Apparent autosomal recessive inheritance in families with proximal spinal muscular atrophy affecting individuals in two generations.
Am J Hum Genet. 1996 Nov;59(5):1163-5.
9
Spinal muscular atrophy: clinical classification and disease heterogeneity.
J Child Neurol. 2007 Aug;22(8):946-51. doi: 10.1177/0883073807305673.
10
Nucleotide differences in SMN1 and SMN2 gene.
Prenat Diagn. 2004 May;24(5):398. doi: 10.1002/pd.843.
Zotero 插件