Papilledema with Camurati-Engelmann disease instigating loss of ganglion cell complex thickness

被引：0

作者：

Satoshi Okimoto

Junichi Kawahara

Yoshiaki Kiuchi

机构：

[1] Hiroshima University Medical School,Department of Ophthalmology

[2] Hiroshima University,Department of Ophthalmology and Visual Science, Graduate School of Biomedical Sciences

来源：

Japanese Journal of Ophthalmology | 2011年 / 55卷

关键词：

Camurati-Engelmann disease; Fourier domain optical coherence tomography; inner retinal layer; papilledema; retinal nerve fiber layer;

D O I：

暂无

中图分类号：

学科分类号：

摘要：

引用

页码：83 / 85

页数：2

共 17 条

[1]

Naveh Y.(1984)Progressive diaphyseal dysplasia: genetics and clinical and radiological manifestations Pediatrics 74 399-405

[2]

Kaftori J.K.(1969)Ocular findings in hereditary diaphyseal dysplasia (Engelmann’s disease) Am J Ophthalmol 68 100-104

[3]

Alon U.(1998)Papilloedema, a complication of progressive diaphyseal dysplasia: a series of three case reports Br J Ophthalmol 82 1042-1048

[4]

Ben-David J.(1991)MR of multiple cranial neuropathies in a patient with Camurati-Engelmann disease: case report Am J Neuroradiol 12 557-559

[5]

Berant M.(1981)Glaucomatous-like visual field defects in chronic papilledema Graefes Arch Clin Exp Ophthalmol 217 99-109

[6]

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