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

Author:

Okimoto Satoshi,Kawahara Junichi,Kiuchi Yoshiaki

Publisher

Springer Science and Business Media LLC

Subject

Ophthalmology,General Medicine

Reference6 articles.

1. Naveh Y, Kaftori JK, Alon U, Ben-David J, Berant M. Progressive diaphyseal dysplasia: genetics and clinical and radiological manifestations. Pediatrics 1984;74:399–405.

2. Morse PH, Walsh FB, McCormick JR. Ocular findings in hereditary diaphyseal dysplasia (Engelmann’s disease). Am J Ophthalmol 1969;68:100–104.

3. Wright M, Miller NR, McFadzean RM, et al. Papilloedema, a complication of progressive diaphyseal dysplasia: a series of three case reports. Br J Ophthalmol 1998;82:1042–1048.

4. Applegate LJ, Applegate GR, Kemp SS. MR of multiple cranial neuropathies in a patient with Camurati-Engelmann disease: case report. Am J Neuroradiol 1991;12:557–559.

5. Grehn F, Knorr-Held S, Kommerell G. Glaucomatous-like visual field defects in chronic papilledema. Graefes Arch Clin Exp Ophthalmol 1981;217:99–109.

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