Chiari I malformation presenting with ganglion cell complex thinning on routine examination
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Conselho Brasileiro De Oftalmologia
Erişim Hakkı
info:eu-repo/semantics/openAccess
Özet
Chiari I malformation (CMI) is a rare congenital disorder characterized by the caudal displacement of cerebellar tonsils through the foramen magnum into the cervical canal(1). Ophthalmological signs include retro-orbital pain, diplopia, photophobia, impaired visual acuity, nystagmus, strabismus, and papilledema(2-4). The diagnosis is mostly based on magnetic resonance imaging (MRI) findings © This content is licensed under a Creative Commons Attributions 4.0 International License.
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Arquivos Brasileiros de Oftalmologia
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85
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4
Künye
Kocamış, Ö., Örnek, K., & Temel, E. (2022). Chiari I malformation presenting with ganglion cell complex thinning on routine examination. Arquivos Brasileiros de Oftalmologia, 85, 435-436.