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Histological, enzymatic and mitochondrial DNA studies in patients with Kearns-Sayre syndrome and chronic progressive external ophthalmoplegia.

作者信息

Reichmann H, Degoul F, Gold R, Meurers B, Ketelsen U P, Hartmann J, Marsac C, Lestienne P

机构信息

Department of Neurology, University of Würzburg, FRG.

出版信息

Eur Neurol. 1991;31(2):108-13. doi: 10.1159/000116656.

DOI:10.1159/000116656
PMID:1646110
Abstract

Kearns-Sayre syndrome has been associated with large heteroplasmic mitochondrial DNA deletions and morphological alterations at the cytological level. We have measured the activities of different respiratory chain complexes in 3 patients presenting mitochondrial DNA deletions and found no close correlation between gene deletions and enzymatic activities. These data, therefore, point out the importance of analyses at the mitochondrial DNA level in such mitochondrial disorders because gross biochemistry may miss any defect.

摘要

相似文献

1
Histological, enzymatic and mitochondrial DNA studies in patients with Kearns-Sayre syndrome and chronic progressive external ophthalmoplegia.
Eur Neurol. 1991;31(2):108-13. doi: 10.1159/000116656.
2
Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome.进行性眼外肌麻痹和凯-赛综合征中的线粒体DNA缺失
N Engl J Med. 1989 May 18;320(20):1293-9. doi: 10.1056/NEJM198905183202001.
3
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Biochem Biophys Res Commun. 1989 Apr 28;160(2):765-71. doi: 10.1016/0006-291x(89)92499-6.
4
Mapping of heteroplasmic mitochondrial DNA deletions in Kearns-Sayre syndrome.卡恩斯-塞尔综合征中异质性线粒体DNA缺失的定位
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Deletions of mitochondrial DNA in Kearns-Sayre syndrome and ocular myopathies: genetic, biochemical and morphological studies.卡恩斯-塞尔综合征及眼肌病中线粒体DNA缺失的遗传、生化及形态学研究
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[Mitochondrial encephalomyopathy].
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Neuro-ophthalmologic manifestations of mitochondrial DNA disorders: chronic progressive external ophthalmoplegia, Kearns-Sayre syndrome, and Leber's hereditary optic neuropathy.线粒体DNA疾病的神经眼科表现:慢性进行性眼外肌麻痹、卡恩斯-塞尔综合征和莱伯遗传性视神经病变。
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8
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9
Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy.与线粒体DNA缺失相关的自发性凯-赛综合征/慢性进行性眼外肌麻痹加综合征:一种滑链复制模型和代谢疗法。
Proc Natl Acad Sci U S A. 1989 Oct;86(20):7952-6. doi: 10.1073/pnas.86.20.7952.
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[Nucleotide mapping and a kinetic model of a heteroplasmic deletion of 4,666 base pairs from mitochondrial DNA in the Kearns-Sayre syndrome].[核苷酸图谱绘制及卡恩斯-塞尔综合征中线粒体DNA 4666个碱基对异质性缺失的动力学模型]
C R Acad Sci III. 1989;309(10):403-7.

引用本文的文献

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Progressive external ophthalmoplegia.进行性眼外肌麻痹。
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2
Diagnosis of Kearns-Sayre Syndrome Requires Comprehensive Work-up.凯-塞尔综合征的诊断需要全面的检查。
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Progressive External Ophthalmoplegia.进行性眼外肌麻痹
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Peripheral neuropathy predicts nuclear gene defect in patients with mitochondrial ophthalmoplegia.周围神经病变可预测线粒体脑肌病伴高乳酸血症和卒中样发作患者的核基因缺陷。
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5
Analyses of energy metabolism and mitochondrial genome in post-mortem brain from patients with Alzheimer's disease.
J Neurol. 1993 Jun;240(6):377-80. doi: 10.1007/BF00839971.
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A topoisomerase II cleavage site is associated with a novel mitochondrial DNA deletion.一种拓扑异构酶II切割位点与一种新的线粒体DNA缺失相关。
Hum Genet. 1995 Jan;95(1):75-81. doi: 10.1007/BF00225079.
7
Molecular biology of neurological diseases.神经疾病的分子生物学
Postgrad Med J. 1992 Apr;68(798):237-41. doi: 10.1136/pgmj.68.798.237.
8
Enzyme activity analyses along ragged-red and normal single muscle fibres.沿破碎红肌纤维和正常单根肌纤维进行酶活性分析。
Histochemistry. 1992 Sep;98(2):131-4. doi: 10.1007/BF00717004.