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Two siblings with nemaline myopathy presenting with rigid spine syndrome.

作者信息

Topaloglu H, Gögüs S, Yalaz K, Kücükali T, Serdaroglu A

机构信息

Department of Paediatric Neurology, Hacettepe University Children's Hospital, Ankara, Turkey.

出版信息

Neuromuscul Disord. 1994 May;4(3):263-7. doi: 10.1016/0960-8966(94)90028-0.

DOI:10.1016/0960-8966(94)90028-0
PMID:7919974
Abstract

Two siblings, ages 20 and 19 presented with more than 10 yr history of spinal rigidity and scoliosis. The parents were first cousins. Muscle biopsies were consistent with nemaline myopathy. This has been the first association between a familial rigid spine syndrome and nemaline myopathy.

摘要

相似文献

1
Two siblings with nemaline myopathy presenting with rigid spine syndrome.
Neuromuscul Disord. 1994 May;4(3):263-7. doi: 10.1016/0960-8966(94)90028-0.
2
Siblings with rigid spine syndrome and nemaline rod myopathy, a unique association.患有僵硬脊柱综合征和杆状体肌病的兄弟姐妹,一种独特的关联。
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[Clinical and pathological studies on nemaline myopathy in adulthood].[成人杆状体肌病的临床与病理研究]
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A new phenotype of autosomal dominant nemaline myopathy.常染色体显性杆状体肌病的一种新表型。
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Nemaline myopathy: current concepts. The ENMC International Consortium and Nemaline Myopathy.杆状体肌病:当前概念。欧洲神经肌肉中心国际联盟与杆状体肌病
J Med Genet. 1997 Sep;34(9):705-13. doi: 10.1136/jmg.34.9.705.
6
[Sibling cases of severe infantile form of nemaline myopathy with ACTA1-gene mutation].[伴有ACTA1基因突变的严重婴儿型杆状体肌病的同胞病例]
No To Hattatsu. 2013 Nov;45(6):452-6.
7
Skeletal muscle repair in a mouse model of nemaline myopathy.在杆状体肌病小鼠模型中的骨骼肌修复
Hum Mol Genet. 2006 Sep 1;15(17):2603-12. doi: 10.1093/hmg/ddl186. Epub 2006 Jul 28.
8
Scoliosis associated with central core disease.与中央轴空病相关的脊柱侧凸
Brain Dev. 1994 Mar-Apr;16(2):150-2. doi: 10.1016/0387-7604(94)90053-1.
9
Clinical and pathological features of patients with nemaline myopathy.杆状体肌病患者的临床和病理特征。
Mol Med Rep. 2014 Jul;10(1):175-82. doi: 10.3892/mmr.2014.2184. Epub 2014 Apr 24.
10
Nebulin is normally expressed in nemaline myopathy.伴肌动蛋白在杆状体肌病中通常会表达。
Acta Neuropathol. 1999 May;97(5):433-6. doi: 10.1007/s004010051011.

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Molecular mechanism of rigid spine with muscular dystrophy type 1 caused by novel mutations of selenoprotein N gene.硒蛋白N基因新突变导致的1型肌营养不良症伴刚性脊柱的分子机制
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Mutations of the selenoprotein N gene, which is implicated in rigid spine muscular dystrophy, cause the classical phenotype of multiminicore disease: reassessing the nosology of early-onset myopathies.
与刚性脊柱肌营养不良相关的硒蛋白N基因突变会导致多微小核病的典型表型:重新评估早发性肌病的分类学。
Am J Hum Genet. 2002 Oct;71(4):739-49. doi: 10.1086/342719. Epub 2002 Aug 21.
4
Identification of a new locus for a peculiar form of congenital muscular dystrophy with early rigidity of the spine, on chromosome 1p35-36.1号染色体p35 - 36区域上一种伴有脊柱早期僵硬的特殊形式先天性肌营养不良新基因座的鉴定。
Am J Hum Genet. 1998 Jun;62(6):1439-45. doi: 10.1086/301882.
5
Nemaline myopathy: current concepts. The ENMC International Consortium and Nemaline Myopathy.杆状体肌病:当前概念。欧洲神经肌肉中心国际联盟与杆状体肌病
J Med Genet. 1997 Sep;34(9):705-13. doi: 10.1136/jmg.34.9.705.