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遗传性视神经病变

Hereditary optic neuropathies.

作者信息

Newman N J, Biousse V

机构信息

Department of Ophthalmology, Emory University School of Medicine, Atlanta, GA 30022, USA.

出版信息

Eye (Lond). 2004 Nov;18(11):1144-60. doi: 10.1038/sj.eye.6701591.

Abstract

AIMS

To provide a clinical update on the hereditary optic neuropathies.

METHODS

Review of the literature.

RESULTS

The hereditary optic neuropathies comprise a group of disorders in which the cause of optic nerve dysfunction appears to be hereditable, based on familial expression or genetic analysis. In some hereditary optic neuropathies, optic nerve dysfunction is typically the only manifestation of the disease. In others, various neurologic and systemic abnormalities are regularly observed.

CONCLUSION

The most common hereditary optic neuropathies are autosomal dominant optic atrophy (Kjer's disease) and maternally inherited Leber's hereditary optic neuropathy. We review the clinical phenotypes of these and other inherited disorders with optic nerve involvement.

摘要

目的

提供遗传性视神经病变的临床最新进展。

方法

文献综述。

结果

遗传性视神经病变包括一组疾病,根据家族性表现或基因分析,视神经功能障碍的病因似乎具有遗传性。在一些遗传性视神经病变中,视神经功能障碍通常是该疾病的唯一表现。在其他病变中,则经常观察到各种神经和全身异常。

结论

最常见的遗传性视神经病变是常染色体显性遗传性视神经萎缩(凯尔病)和母系遗传的莱伯遗传性视神经病变。我们综述了这些以及其他累及视神经的遗传性疾病的临床表型。

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