莱伯遗传性视神经病变合并肌张力障碍 - Suppr

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Leber optic hereditary neuropathy plus dystonia.

作者信息

Mahoui S, Belkhamsa O, Ait Kaci I, Abada Bendib M, Castelnovo G

机构信息

Department of neurology, university hospital of Ben Aknoun, Algiers, Algeria.

Department of neurology, university hospital Nedir Mohamed, Tizi Ouzou, Algeria.

出版信息

Rev Neurol (Paris). 2019 Sep-Oct;175(7-8):483-484. doi: 10.1016/j.neurol.2018.12.011. Epub 2019 Jun 17.

DOI:10.1016/j.neurol.2018.12.011

PMID:31221418

Abstract

摘要

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相似文献

Leber optic hereditary neuropathy plus dystonia.

Rev Neurol (Paris). 2019 Sep-Oct;175(7-8):483-484. doi: 10.1016/j.neurol.2018.12.011. Epub 2019 Jun 17.

A case of Leber hereditary optic neuropathy plus dystonia caused by G14459A mitochondrial mutation.

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Recurrent visual loss in Leber hereditary optic neuropathy.

Arch Ophthalmol. 2003 Feb;121(2):288-91. doi: 10.1001/archopht.121.2.288.

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Brain. 2009 Sep;132(Pt 9):2306-8. doi: 10.1093/brain/awp195.

Late-onset Leber hereditary optic neuropathy.

Clin Exp Ophthalmol. 2013 Sep-Oct;41(7):690-3. doi: 10.1111/ceo.12091. Epub 2013 Apr 11.

Nuclear DNA Mutation Causing a Phenotypic Leber Hereditary Optic Neuropathy Plus.

Ophthalmology. 2021 Apr;128(4):628-631. doi: 10.1016/j.ophtha.2020.09.011. Epub 2020 Sep 9.

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J Neuroophthalmol. 2013 Sep;33(3):276-8. doi: 10.1097/WNO.0b013e31828f8d75.

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