- Acquired Unilateral Night Blindness
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Lee HJ, Seo JH, Koo HM, Chung SK
- KMID: 2147607
- J Korean Ophthalmol Soc.
- 2000 Jan;41(1):276-281.
Night blindness is not an uncommon symptom and may occur in a wide variety of disease.However, the occurrence of acquired unilateral night blindness that has no specific clinical symptoms and... -
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- Congenital Stationary Night Blindness with Myopia
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Son JY, Hwang BN, Yang JW, Yun IH
- KMID: 2206660
- J Korean Ophthalmol Soc.
- 2003 Aug;44(8):1931-1935.
PURPOSE: To report a case of Congenital stationary night blindness associated with myopia. METHODS: A 19-year-old male with night blindness was referred to our hospital. We studied patient's family history,... -
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- A Case of Oguchi's Disease
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Kim HT, Lim SJ, Kim JW
- KMID: 1949821
- J Korean Ophthalmol Soc.
- 1990 Jan;31(1):105-109.
Oguchi's disease is an unusual form of congenital stationary night blindness that is characterized by a peculiar grey-white discoloration of the retina that gives a metallic sheen. After prolonged dark... -
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- Night Blindness Induced by Long-term External Bile Drainage
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Lee SM, Choi JY, Kang HJ, Sung JH, Park SJ, Yoo SH, Park YM
- KMID: 2171328
- Ewha Med J.
- 2015 Mar;38(1):42-45.
- doi: 10.12771/emj.2015.38.1.42
Vitamin A deficiency can occur as a result of malnutrition, malabsorption, or poor vitamin metabolism due to liver disease and night blindness might develop as the first symptom. Although there... -
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- A Case of Retinitis Pigmentosa without Pigment
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Baek JH, Lee CY, Kim JH, Ma JK
- KMID: 1948773
- J Korean Ophthalmol Soc.
- 1981 Jun;22(2):457-462.
Retinitis pigmentosa without pigment is a varient of retinitis pigmentosa which is a hereditory disorder. It is characterized by decreased visual acuity, night blindness and contraction of visual field in... -
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- The Electrophysiologic Diagnosis of Congenital Stationary Night Blindness
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Jo YS, Kim SY, Kim SY
- KMID: 2204825
- J Korean Ophthalmol Soc.
- 1987 Oct;28(5):1063-1070.
An analysis of four patients with congenital stationary night blindness showed that all had essentially normal fundi. We studied electro physiologic examinations including electroretinogram(ERG), electrooculogram(EOG) and pattern visual evoked potential(VEP).... -
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- A Case of Retinitis Punctata Albescens
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Kang CK, Lee TS
- KMID: 2204721
- J Korean Ophthalmol Soc.
- 1982 Sep;23(3):773-777.
Retinitis Punctata Albescens is a condition characterized by night blindness and the presence of multiple small discrete white dots scattered over the fundus except in the macular area. Progressive form... -
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- Choroideremia
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Lee CY, Shin TY
- KMID: 1948769
- J Korean Ophthalmol Soc.
- 1981 Jun;22(2):433-438.
Choroideremia is characterized by progressive atrophy of choroid and pigment epithelium of retina leading to night blindness and gross loss of field. and is inherited as X chromosome linked intermediate.... -
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- A Case of Choroideremia with Recurrent Anterior Uveitis
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O SJ, Kim SH, Lee HY
- KMID: 754343
- Korean J Ophthalmol.
- 2003 Jun;17(1):55-62.
- doi: 10.3341/kjo.2003.17.1.55
Choroideremia is a rare hereditary disease with characteristic fundus that causes night blindness and peripheral visual field loss. The authors encounter choroideremia accompanied by recurrent uveitis. This paper is designed... -
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- A Case of Unilateral Retinitis Pigmentosa
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Kim KH, Park YH, Hahn DK
- KMID: 2022646
- J Korean Ophthalmol Soc.
- 1996 Jun;37(6):1090-1094.
Retinitis pigmentosa has been recognized as a symmetrical, bilateral, hereditary, tapetoretinal degeneration with night blindness, visual field loss, and abnormal ERG. Unilateral retinitis pigmentosa is a rather rare disease. Pedraglia... -
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- The Classification and Multifocal ERG Findings of Congenital Stationary Night Blindness
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Sung MS, Park TK, Ohn YH
- KMID: 2337235
- J Korean Ophthalmol Soc.
- 2005 Nov;46(11):1936-1943.
PURPOSE: To report on the classification of congenital stationary night blindness (CSNB) and multifocal ERG findings. METHODS: We studied three patients (case 1-3) with night blindness but normal fundus and... -
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- Type IV Ushers Syndrome Manifested by Woman
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Kim SH, Koo HM, Chung SK
- KMID: 1952501
- J Korean Ophthalmol Soc.
- 1997 Jul;38(7):1289-1293.
Ushers syndrome is an autosomal recessively inherited trait that characterized by progressive retinitis pigmentosa combining night blindness with a congenital, nonprogressive sensorineural hearing impairment of variable severity. Speech disorder, vestibular... -
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- A Case of Laurence-Moon-Biedl Syndrome
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Chi NC
- KMID: 2122561
- J Korean Ophthalmol Soc.
- 1975 Mar;16(1):85-88.
A case of Laurence-Moon-Biedl Syndrome in 13-year-old Korean boy was reported with some clinical observation. Visual disturbance and night blindness were his chief complaints for about 3 years prior to... -
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- Specific Spectral Domain Optical Coherence Tomographic Findings of Oguchi Disease
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Hyun J, Park TK, Chang JH, Ohn YH
- KMID: 2215869
- J Korean Ophthalmol Soc.
- 2012 Jul;53(7):1041-1045.
- doi: 10.3341/jkos.2012.53.7.1041
PURPOSE: To report specific spectral domain OCT findings of Oguchi disease diagnosed with fundoscopic examination and electrophysiological study. CASE SUMMARY: A 14-year-old patient visited our clinic with a complaint of night... -
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- Two Cases of Amaurosis Hysterica
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Shin JS
- KMID: 1676025
- J Korean Ophthalmol Soc.
- 1962 Jan;3(1):37-40.
Two cases of hysteric amaurosis are reported. The first case is a male, 38 years of age, who had suffered from hysteric amaurosis three times during the last three years.... -
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- Identification of Pathogenic Variants in the CHM Gene in Two Korean Patients With Choroideremia
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Bae K, Song JS, Lee C, Kim NK, Park WY, Kim BJ, Ki CS, Kim SJ
- KMID: 2383921
- Ann Lab Med.
- 2017 Sep;37(5):438-442.
- doi: 10.3343/alm.2017.37.5.438
Choroideremia is a rare X-linked disorder causing progressive chorioretinal atrophy. Affected patients develop night blindness with progressive peripheral vision loss and eventual blindness. Herein, we report two Korean families with... -
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- Retinitis Pigmentosa Complicated by Vitreous Hemorrhage in a Young Patient: A Case Report
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Chung IY, Huh HD, Kim SJ, Han YS, Seo SW, Park JM
- KMID: 2338388
- J Korean Ophthalmol Soc.
- 2013 Aug;54(8):1293-1297.
PURPOSE: To report a case of a young male patient with retinitis pigmentosa (RP) accompanied by vitritis and neovascularization of the optic disk in both eyes who underwent unilateral vitrectomy... -
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- Two Female Siblings With Bietti Crystalline Retinopathy Without Corneal Dystrophy
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Ha SM, Yu HG
- KMID: 2212505
- J Korean Ophthalmol Soc.
- 2009 Jul;50(7):1120-1127.
- doi: 10.3341/jkos.2009.50.7.1120
PURPOSE: To report clinical and functional results in two female siblings with Bietti crystalline retinopathy. CASE SUMMARY: Recently, a 48-year-old female with bilateral intraretinal depositions presented with a complaint of... -
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- The Effect of Cytochrome C in Ophthalmic Diseases
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Kim HC, Kim JJ, Pak BG
- KMID: 1675861
- J Korean Ophthalmol Soc.
- 1968 Mar;9(1):1-8.
Cytochrome compounds which act as electron transfer agents in oxidation-reduction reactions. An important example is cytochrome c, which has a molecular weight of about 13,000 and contains one atom of... -
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- A Case of Gyrate Atrophy of Choroid and Retina
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Sim WH, Lim BO, Kim SY
- KMID: 2204797
- J Korean Ophthalmol Soc.
- 1986 Aug;27(4):693-699.
Gyrate atrophy of choroid and retina is a rare hereditary disorder, which is characterized by progressive decrease of visual acuity, nyctalopia, visual field constriction and posterior subcapsular cataract. The authors... -
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