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神经眼科遗传学

Neuro-ophthalmic genetics.

作者信息

Kerrison J B, Maumenee I H

机构信息

Wilmer Eye Institute, Johns Hopkins Center for Hereditary Eye Diseases, Johns Hopkins Hospital, Baltimore, MD 21287, USA.

出版信息

Curr Opin Ophthalmol. 1997 Dec;8(6):35-40. doi: 10.1097/00055735-199712000-00006.

Abstract

Mutations in nuclear or mitochondrial DNA may cause disorders of neuro-ophthalmic significance. These include disorders of the optic nerve, such as Leber's hereditary optic neuropathy and Kjer-type optic atrophy, and disorders of ocular motility, such as congenital nystagmus, autosomal dominant progressive external ophthalmoplegia, and oculopharyngeal muscular dystrophy. In addition to more accurate disease classification and diagnosis, identification of genetic loci, genes, and their mutations has stimulated investigation into factors influencing disease expression and penetrance.

摘要

核DNA或线粒体DNA的突变可能导致具有神经眼科意义的疾病。这些疾病包括视神经疾病,如Leber遗传性视神经病变和Kjer型视神经萎缩,以及眼球运动障碍,如先天性眼球震颤、常染色体显性进行性眼外肌麻痹和眼咽型肌营养不良。除了更准确的疾病分类和诊断外,基因位点、基因及其突变的识别还激发了对影响疾病表现和外显率的因素的研究。

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