- Aniridia Intraocular Lens
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Seo MS, Lim ST
- KMID: 2108032
- J Korean Ophthalmol Soc.
- 1996 Feb;37(2):233-236.
We implanted aniridia intraocular lenses (aniridia IOL) on three cases with complaint of glare caused by traumatic or congenital aniridias combined with cataract or aphakia. Aniridia IOLs were fixed by... -
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- A Case of Congenital Aniridia
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Kwak PS
- KMID: 2107249
- J Korean Ophthalmol Soc.
- 1978 Jun;19(2):221-225.
The author have experienced a case of aniridia in a 44 year-old man. Aniridia is an uncommon congenital anomaly, is almost bilateral cmd appears as a dominant characteristic. Coincident anomalies... -
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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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- Congenital Aniridia in a Family for Three Generations
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Lee JI, Kim YH, Ahn CS
- KMID: 1949771
- J Korean Ophthalmol Soc.
- 1990 Mar;31(3):383-389.
Aniridia is a congenital, often hereditary, usually bilateral absence of iris in whole or in part. And aniridia occurs mainly as an autosomal dominant condition with almost complete penetrance. In... -
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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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- Three Cases of Congenital Aniridia in One Family
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Bae JH, Cho YW, Kwak MS
- KMID: 2147608
- J Korean Ophthalmol Soc.
- 2000 Jan;41(1):282-287.
Aniridia is a relatively rare congenital anomaly and its incidence is about 1:100, 000.Main features of aniridia include congenitally partial or nearly complete absence of the iris and hypoplasia of... -
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- A Case of Aniridia
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Chung SJ
- KMID: 1658331
- J Korean Ophthalmol Soc.
- 1971 Sep;12(3):119-120.
The author experienced a case of Aniridia in both eyes with increased intra-ouclar pressure. She was 3 month old and had no other congenital abnormalities and significant family history. Intra-ouclar... -
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- A Case of Traumatic Complete Aniridia with Corneal Laceration
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Song KS, Yi GY
- KMID: 2205954
- J Korean Ophthalmol Soc.
- 2000 Sep;41(9):2013-2017.
Traumatic aniridia is usually accompanied by severe anterior segment disruption including corneal laceration, cataract, and vitreous prolapse into the anterior chamber. We experienced a case of complete traumatic aniridia following... -
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- Two Cases of Congenital Aniridia
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Hong KY, Chung YT
- KMID: 2122756
- J Korean Ophthalmol Soc.
- 1987 Aug;28(4):851-857.
Aniridia, the bilateral total or partial absence of the iris, is a rare congenital often hereditary anomaly which usually leads to blindness in adulthood due to secondary glaucoma and cataract... -
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- The Congenital Aniridia in One Family
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Cho YA
- KMID: 1948894
- J Korean Ophthalmol Soc.
- 1979 Mar;20(1):113-118.
Aniridia or irideremia is characterized by reduction of iris or absence of total iris, but a rudimentary iris is always present in most cases. This congenital anomaly is familial and... -
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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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- Clinical Results of Black-Diaphragm Intraocular Lens Implantation
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Choi DW, Chung IY, Seo SW, Song JK
- KMID: 2337170
- J Korean Ophthalmol Soc.
- 2004 Nov;45(11):1851-1857.
PURPOSE: We studied the clinical products of sulcus fixation of Black-diaphragm intraocular lens and transscleral fixation of Black-diaphragm intraocular lens in congenital and acquired aniridia patients. METHODS: We retrospectively analyzed... -
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- PAX6 Mutations and Clinical Features of Congenital Aniridia
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Kim JH, Hwang BS, Lee JH, Cha SC
- KMID: 2337738
- J Korean Ophthalmol Soc.
- 2008 Nov;49(11):1794-1800.
PURPOSE: To report the PAX6 mutations and clinical features in Korean aniridia patients. METHODS: Genomic DNA was isolated from 12 aniridia patients and 5 normal controls. The coding regions of the... -
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- A Case of Isolated Traumatic Aniridia in a Pseudophakic Eye
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Kwon MY, Hong HJ, Park DJ
- KMID: 2428692
- J Korean Ophthalmol Soc.
- 2018 Dec;59(12):1185-1189.
- doi: 10.3341/jkos.2018.59.12.1185
PURPOSE: We report a rare case of isolated traumatic aniridia in a pseudophakic eye. CASE SUMMARY: A 69-year-old female came to our emergency department complaining of right eye pain and visual... -
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- A nonsense PAX6 mutation in a family with congenital aniridia
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Han KH, Lee HJ, Ha IS, Kang HG, Cheong HI
- KMID: 2362243
- Korean J Pediatr.
- 2016 Nov;59(Suppl 1):S1-S4.
- doi: 10.3345/kjp.2016.59.11.S1
Congenital aniridia is a rare ocular malformation that presents with severe hypoplasia of the iris and various ocular manifestations. Most cases of congenital aniridia are known to be related to... -
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- Wilms' tumor, aniridia, genitourinary anomalies, and mental retardation (WAGR) syndrome: Successful treatment of the first case with bilateral Wilms' tumors in Korea
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Min KS, Baek HJ, Han DK, You JH, Hwang TJ, Kwon DD, Kook H
- KMID: 1494529
- Korean J Pediatr.
- 2008 Dec;51(12):1355-1358.
- doi: 10.3345/kjp.2008.51.12.1355
Wilms' tumor, aniridia, genitourinary anomalies, and mental retardation (WAGR) syndrome is caused by deletion of chromosome 11p13, including the Wilms' tumor (WT1) and aniridia gene (PAX6) loci. Here, we report... -
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- Gillespie Syndrome with Partial Aniridia, Cerebellar Ataxia, Delayed Development: A case report
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Chang SK, Oh HI, Yoo YJ, Ahn SH, Jang IH
- KMID: 2323183
- J Korean Acad Rehabil Med.
- 1999 Feb;23(1):181-185.
In 1965 Gillespie reported a new syndrome of bilateral aniridia, cerebellar ataxia, and oligophrenia (mental retardation). This new syndrome was named Gillespie syndrome. Since then only 17 cases of Gillespie... -
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- Implantation of Black Diaphragm Intraocular Lens in Cataract Surgery with Congenital Aniridia
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Park SJ, Kim HT, Kim SM, Chung SK
- KMID: 2108519
- J Korean Ophthalmol Soc.
- 1998 Aug;39(8):1748-1754.
Cogenita aniridia is a relatively rare congenital anomay and its incidence is about 1:100,000. It occurs along with cataract(85%) and nystagmus(92%). Black diaphragm intraocular lenses(IOLs) were inserted in five eyes... -
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- A Case of Anterior Fibrovascular Membrane After Intraocular Lens Implantation in Congenital Aniridia
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Lee KS, Moon JW, Park JW, Choi JH
- KMID: 2211716
- J Korean Ophthalmol Soc.
- 2008 May;49(5):835-839.
- doi: 10.3341/jkos.2008.49.5.835
PURPOSE: To report a case of an anterior fibrovascular membrane following cataract extraction and intraocular lens implantation in a patient with congenital aniridia. CASE SUMMARY: A 13-year-old girl presented with congenital... -
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- The Congenital Aniridia in Mother and her two Sons
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Rhee ST, Hong KS, Sohn MS, Choi CS
- KMID: 2336334
- J Korean Ophthalmol Soc.
- 1971 Dec;12(4):199-202.
Aniridia or iridremis is a Clinical term denoting absence of the iris in whole or in part. Actually, total absence has not been reported, as there has been rudimentary iris... -
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