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Leber hereditary optic neuropathy--a disease with a known molecular basis but a mysterious mechanism of pathology.

作者信息

Mroczek-Tońska Katarzyna, Kisiel Bartłomiej, Piechota Janusz, Bartnik Ewa

机构信息

Department of Genetics, University of Warsaw, Warszawa, Poland.

出版信息

J Appl Genet. 2003;44(4):529-38.

PMID:14617834
Abstract

Leber hereditary optic neuropathy is a maternally inherited type of blindness caused by degeneration of the optic nerve. It is caused by point mutations in mitochondrial DNA. Like in other mitochondrial diseases, its penetrance and inheritance is complicated by heteroplasmy, tissue distribution, and the bottleneck phenomenon in oocyte maturation. On the cellular level, the mechanism of the disease development is still mysterious. Currently three theories of pathomechanism of LHON are considered: biochemical, ROS (reactive oxygen species) and apoptotic.

摘要

相似文献

1
Leber hereditary optic neuropathy--a disease with a known molecular basis but a mysterious mechanism of pathology.
J Appl Genet. 2003;44(4):529-38.
2
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Mitochondrial abnormalities in patients with LHON-like optic neuropathies.LHON样视神经病变患者的线粒体异常
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[Genetic basis of hereditary optic atrophies].[遗传性视神经萎缩的遗传基础]
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Leber's hereditary optic neuropathy: a multifactorial disease.莱伯遗传性视神经病变:一种多因素疾病。
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Heteroplasmy analysis in the Polish patients with 11778A mutation responsible for Leber hereditary optic neuropathy.对患有由11778A突变导致的Leber遗传性视神经病变的波兰患者进行异质性分析。
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[The influence of mitochondrial haplogroup on Leber's hereditary optic neuropathy].[线粒体单倍群对Leber遗传性视神经病变的影响]
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Mutations for Leber hereditary optic neuropathy in patients with alcohol and tobacco optic neuropathy.酒精性和烟草性视神经病变患者中与Leber遗传性视神经病变相关的突变。
Mol Vis. 2011;17:3175-9. Epub 2011 Dec 7.