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作 者:Jennifer Enright Gregory Van Stavern
出 处:《Annals of Eye Science》2020年第2期69-81,共13页眼科学年鉴(英文)
基 金:This work was supported by an unrestricted grant from the Research to Prevent Blindness to the Washington University Department of Ophthalmology and Visual Sciences,and by a Research Award from the Vitreoretinal Surgery Foundation(JE).
摘 要:Hereditary,metabolic and toxic optic neuropathies cause bilateral,central vision loss and therefore can result in severe impairment in visual function.Accurate,early diagnosis is critical,as nutritional and toxic optic neuropathies may be reversible if identified early,and diagnosis of hereditary optic neuropathies can prevent unnecessary invasive workup,provide prognostic information,and allow for effective genetic counseling.Optical coherence tomography(OCT)is a valuable tool that aids in the diagnosis and prognostication of optic neuropathies as it allows for quantification of changes in the retinal ganglion cells(RGCs)and retinal nerve fiber layer(RNFL)over time.We review the characteristic clinical presentations of hereditary,metabolic and toxic optic neuropathies,with an emphasis on OCT findings.
关 键 词:Optical coherence tomography(OCT) optic neuropathy Leber hereditary optic neuropathy(LHON) autosomal dominant optic atrophy(ADOA) ETHAMBUTOL
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