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Dominant Optic Atrophy Caused by the c.1334G>A Mutation of the OPA1 Gene

Choi YS, Oh JH, Hwang SK, Chun BY

Purpose: Dominant optic atrophy is one of the most common hereditary optic neuropathies, causing progressive bilateral vision loss that begins early in life. Optic atrophy 1 (OPA1) gene mutation brings...
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Bilateral Ocular Toxoplasmosis that Caused Optic Atrophy Secondary to Papillitis

Lee D, Kim M, Moon JW

Purpose: We report a case of ocular toxoplasmosis that caused bilateral optic atrophy secondary to papillitis. Case summary: A 52-year-old male with no history of systemic disease was referred to our...
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Retinal Ganglion Cell Layer Thicknesses and Visual Functions in Patients with Bilateral Temporal Optic Atrophy

Kim BG, Park JY, Oh WH, Choi J

PURPOSE: To investigate correlations between macular retinal ganglion cell (RGC) layer thickness and best-corrected visual acuity (BCVA) and visual field parameters in patients with bilateral temporal optic atrophy. METHODS: Thirty eyes...
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A Case of Leber Hereditary Optic Neuropathy Showing Optic Disc Hyperfluorescence

Park YJ, Lim HT

PURPOSE: We report an unusual case of Leber hereditary optic neuropathy presenting with optic disc hyperfluorescence. CASE SUMMARY: A 17-year-old male with sequential painless visual loss 3 weeks apart affecting first...
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Septo-optic dysplasia plus diagnosed in a middle-aged woman

Oh ST, Kang MR, Oh SI, Kim EG, Kim SJ, Seo JH, Chung EJ, Ji KH

Septo-optic dysplasia is a congenital anomaly with diverse phenotypes from normal to mixtures of visual abnormality, endocrine dysfunction, psychomotor retardations and epileptic seizures. It is characterized by optic atrophy, pituitary...
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A Case of Atypical Leber Hereditary Optic Neuropathy Associated with MT-TL1 Gene Mutation Misdiagnosed with Glaucoma

Hahn IK, Lim HT

PURPOSE: Leber hereditary optic neuropathy (LHON) is one of the most common hereditary optic neuropathies caused by mutations of mitochondrial DNA. Three common mitochondrial mutations causing LHON are m.3460, m.11778,...
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Influence of RNFL Thickness on Visual Acuity and Visual Field in Bilateral Temporal Optic Atrophy

Park JY, Choi J, Oh WH, Kim JS

PURPOSE: To investigate the influence of retinal nerve fiber layer (RNFL) thickness on visual acuity and visual field in patients with bilateral temporal optic atrophy. METHODS: Patients with characteristic features of...
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A Case of Optic Atrophy and Visual Field Defect in Periventricular Leukomalacia

Kim HY, Choi HY, Lee JW

PURPOSE: To report a case of visual field defect and optic atrophy in a patient with periventricular leukomalacia. CASE SUMMARY: A 22-year-old woman was referred to our hospital for further glaucoma...
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Optic Disc Atrophy in Patient with Posner-Schlossman Syndrome

Kim TH, Kim JL, Kee C

A 32-year-old man with blurred vision in the right eye and headache presented with anterior uveitis, an intraocular pressure (IOP) of 60 mmHg, an open angle, no visual field defects,...
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A Case of Optic Nerve Atrophy with Severe Disc Cupping after Methanol Poisoning

Shin YW, Uhm KB

We report a rare case of optic nerve atrophy with severe disc cupping resulting from methanol poisoning. A 30-year-old man presented to the hospital complaining of decreased visual acuity in...
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Ocular Findings in Patients with Fibrous Dysplasia

Kim NJ, Wang KC, Kim SW, Son WG, Hwang JM

  • KMID: 2337379
  • J Korean Ophthalmol Soc.
  • 2006 May;47(5):787-798.
PURPOSE: Fibrous dysplasia is an uncommon disease that replaces normal bone tissue with fibrous and osteoid tissue. We evaluated patients with fibrous dysplasia involving orbital bones to identify the ocular...
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A Case Refort of Sandhoff Disease

Yun YM, Lee SN

Sandhoff disease is a rare autosomal recessive metabolic disease presenting bilateral optic atrophy and a cherry red spot in the macula. This case report presents the characteristics of a patient...
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A case of retained wooden foreign body in orbit

Lee JA, Lee HY

A 41-year-old man visited our clinic complaining of esodeviation of the right eye. He had been operated on for corneal laceration 3 years before. One month later, exodeviation of the...
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Leber's Hereditary Optic Neuropathy with 3460 Mitochondrial DNA Mutation

Hwang JM, Chang BL, Koh HJ, Kim JY, Park SS

Leber's hereditary optic neuropathy (LHON) is a maternally transmitted disease causing acute or subacute, bilateral optic atrophy mainly in young men. It is found to be a mitochondrial disorder with...
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Analysis of 137 Pediatric Low Vision Patients

Park MG, Moon NJ

  • KMID: 2124982
  • J Korean Ophthalmol Soc.
  • 2001 Aug;42(8):1194-1201.
PURPOSE: We intended to analyze the characteristics of a pediatric low vision population. METHODS: Among 430 patients who visited our low vision clinic from May 1995 to April 2000, 137...
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Autosomal Dominant Cerebellar Ataxia Type II Associated with Optic Atrophy

Kim IT, Shim SD

  • KMID: 2205379
  • J Korean Ophthalmol Soc.
  • 1998 Oct;39(10):2494-2498.
Autosomal dominant cerebellar ataxia(ADCA) is an unusual, familial hereditary disorder that ha been called olivopontocerebellar atrophy. ADCA type II is usually accompanied with severely decreased visual acuity and cerebellar ataxia....
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Visual Rehabilitation of Optic Atrophy Patients with Low Vision Aids

Kim JW, Chang SI, Moon NJ

  • KMID: 2336618
  • J Korean Ophthalmol Soc.
  • 1997 Mar;38(3):450-457.
In oder to evaluate the efficacy of low vision aids in patients with optic atrophy, we analyzed sex, age distribution, preexisting conditions, visual acuities before and after low vision aids...
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A Case of Optic Atrophy following Methanol Poisoning

Song MS, Yoon BJ

  • KMID: 1949553
  • J Korean Ophthalmol Soc.
  • 1989 Dec;30(6):1021-1024.
Methanol poisoning is a rare disease but may cause blindness and, in severe cases, results in death. It may develop lesions in optic nerve and retina, which may be accompanied...
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