- Three Cases of Simple Ectopia Lentis in One Family
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Hong KY, Joh SC, Chung YT
- KMID: 2122723
- J Korean Ophthalmol Soc.
- 1986 Oct;27(5):867-873.
Ectopia lentis, Synonymously with Congenital dislocated lens, is defined as a dislocation of the ocular lens, of greater or less degree, based on a developmental anomaly. It occurs in three... -
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- Transscleral IOL Fixation With Preserved Anterior Vitreous Face in Marfan Syndrome With Ectopia Lentis
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Choi HW, Kim EH, Kim WS
- KMID: 2212530
- J Korean Ophthalmol Soc.
- 2009 Aug;50(8):1174-1178.
- doi: 10.3341/jkos.2009.50.8.1174
PURPOSE: To evaluate the safety and efficacy of transscleral intraocular lens (IOL) fixation while preserving the anterior vitreous face in treating ectopia lentis of Marfan syndrome. METHODS: This study included... -
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- Management of Ectopia Lentis in Children
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Yu YS, Awh JY, Lee JH
- KMID: 2124316
- J Korean Ophthalmol Soc.
- 1999 Jul;40(7):1973-1978.
To know the causes and visual prognosis of ectopia lentis in children, medical records of 41 patients (82 eyes) were retrospectively analysed.The patients were divided into systemic disease-associated, simple, and... -
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- Long Term Results of the Lensectomy in Children with Ectopia Lentis
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Kim SY, Kim SJ, Yu YS
- KMID: 2207644
- J Korean Ophthalmol Soc.
- 2005 Feb;46(2):250-256.
PURPOSE: To analyze the clinical features and the long term visual results of children with ectopia lentis after lensectomy. METHODS: Enrolled in this study were 79 eyes of 43 patients... -
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- Phacoemulsification Using Microhook Iris Retractor for the Management of Ectopia Lentis in Marfan Syndrome
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Oh HS, Koh HJ, Kim CY, Lim SJ
- KMID: 2337013
- J Korean Ophthalmol Soc.
- 2002 Jun;43(6):993-999.
PURPOSE: We evaluated the clinical results of phacoemulsifacation using microhook iris retractor for the management of ectopia lentis in Marfan syndrome. METHODS: Seventeen eyes of 9 patients with Marfan syndrome were... -
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- A Case of Homocystinuria with Ectopia Lentis
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Chung DY, Chung YT
- KMID: 2122983
- J Korean Ophthalmol Soc.
- 1991 Jan;32(1):110-115.
Homocystinuria is an inborn error on the pathway of the methionine metabolism. It is mainly caused by a cystathionine B-synthase deficiency in the brain or liver. Homocystinuria is biochemically characterized... -
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- A Case of Congenital Aniridia
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Ahn SK, Kang JS, Shyn KH
- KMID: 2107594
- J Korean Ophthalmol Soc.
- 1989 Oct;30(5):815-818.
Aniridia, a condition which shows only an extremely rudimentary iris, is a re latively rare congenital anomaly. It is almost bilateral and occurs as an autosomal dominant trait. The authors... -
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- The Visual Prognosis in Marfan Syndrome with Ectopia Lentis
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Yang JW, Kim HS, Lee YC
- KMID: 2206197
- J Korean Ophthalmol Soc.
- 2002 Oct;43(10):1876-1881.
PURPOSE: To assess the clinical characteristics, indications of operation, operative methods and visual prognosis in Marfan syndrome with ectopia lentis. METHODS: Medical records of 13 patients (24 eyes) operated due to... -
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- A Case of Madan's Syndrome
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Shyn KH, Chang WU, Kim SY, Seon DK
- KMID: 2107230
- J Korean Ophthalmol Soc.
- 1977 Mar;18(1):143-145.
Marfan's syndrome is another name of arachnodactyly and was firstly noted by Marfan in 1896. Salle found that ocular signs are also accompanied by this syndrome. Since then, many cases... -
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- Congenital Aniridia
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Lee KH, Lee JK
- KMID: 2205048
- J Korean Ophthalmol Soc.
- 1995 Mar;36(3):535-539.
Aniridia is a very rare disorder the main features of which are congenitally partial or nearly complete absence of the iris and foveal hypoplasia. The authors obseved aniridia in two... -
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- Identification of a Fibrillin-1 Gene Mutation in a Monozygotic Twin Presenting with Bilateral Juvenile-onset Ectopia Lentis
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Yum HR, Kim SE, Shin SY, Park SH
- KMID: 2360145
- Korean J Ophthalmol.
- 2015 Feb;29(1):77-78.
- doi: 10.3341/kjo.2015.29.1.77
No abstract available. -
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- Bilateral Simple Ectopia Lentis Associated with FBN1 Gene Mutation
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Nam SW, Song JS, Ki CS, Kee CW
- KMID: 2393174
- J Korean Ophthalmol Soc.
- 2017 Oct;58(10):1199-1204.
- doi: 10.3341/jkos.2017.58.10.1199
PURPOSE: To report a case of bilateral simple ectopia lentis associated with FBN1 gene mutation. CASE SUMMARY: A 47-year-old women presented with a one-month history of ocular pain and decreased visual... -
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- One Family of Aniridia
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Hwang YJ, Kim BH, Bae HB, Shim WS
- KMID: 1665747
- J Korean Ophthalmol Soc.
- 1980 Sep;21(3):255-259.
Aniridia is a congenital lack of iris and rudimentary iris tissue, almost always bilateral, occuring as a dominant characteristic by an autosomal gene with high penetrance and variable expression. The... -
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- A Case of Homocystinuria Complicated with Systemic Deep Vein Thrombosis and Venous Infarction of Thalamus
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Kang JH, Koo NH, Kim SH, Cho JH, Kim SY
- KMID: 2177057
- J Korean Child Neurol Soc.
- 2002 Nov;10(2):344-350.
Homocystinuria is an autosomal recessive inherited disorder of methionine metabolism. The most common cause of homocystinuria is cystathione-beta-synthase deficiency, which has the characteristic clinical features such as ectopia lentis, Marfanoid... -
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- Clinical Characteristics of Marfan Syndrome in Korea
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Lim AY, Song JS, Kim EK, Jang SY, Chung TY, Choi SH, Sung K, Huh J, Kang IS, Choe YH, Ki CS, Kim DK
- KMID: 2355461
- Korean Circ J.
- 2016 Nov;46(6):841-845.
- doi: 10.4070/kcj.2016.46.6.841
BACKGROUND AND OBJECTIVES: Marfan syndrome (MFS) is a connective tissue disorder with autosomal dominant inheritance and a highly variable clinical spectrum. However, there are limited data available on the clinical... -
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- Atypical Neonatal Marfan Syndrome with p.Glu1073Lys Mutation of FBN1: the First Case in Korea
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Heo JS, Song JY, Choi EY, Kim EH, Kim JH, Park SE, Jeon JH
- KMID: 2417577
- J Korean Med Sci.
- 2017 Jan;32(1):1-3.
- doi: 10.3346/jkms.2017.32.1.1
Neonatal Marfan syndrome (nMFS) is considered to be on the most severe end of the spectrum of type I fibrillinopathies. The common features of nMFS include ascending aortic dilatation, severe... -
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- The Clinical Study on Marfan Syndrome
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Kim JS, Jin DK, Ko SH, Min JY, Kang IS, Jeon KW, Choi YL, Lee HJ, Park SW, Lee WR, Lee CS, Oh SY, Ki CW, Yoo HW, Park IS, Ko JK
- KMID: 2104410
- J Korean Pediatr Soc.
- 1998 Oct;41(10):1411-1416.
PURPOSE: The aim of this study was to assess the involvement of several organs patients with Marfan syndrome in Korea. Also the clinical features in childhood patients with Marfan syndrome... -
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