Skip Navigation
Skip to contents
Results by Year

View Wide

Filter

ARTICLE TYPE

PUBLICATION DATE

5 results
Display

A Korean Patient with Lattice Corneal Dystrophy Type IV with Leu527Arg Mutation in the TGFBI Gene

Kim J, Lee KA, Kim EK, Lee HK

An 87-year-old woman visited our clinic for a scheduled cataract surgery. At the time of preoperative evaluation, slit lamp examination showed lattice-shaped and granular deposits with asymmetrical patterns in the...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Korean Patient with Macular Corneal Dystrophy Associated with Novel Mutation in the CHST6 Gene

Lee YK, Chang DJ, Chung SK

To report a novel mutation within the CHST6 gene, as well as describe light and electron microscopic features of a case of macular corneal dystrophy. A 59-year old woman with...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Novel Decorin Gene Mutation in Congenital Hereditary Stromal Dystrophy: A Korean Family

Lee JH, Ki CS, Chung ES, Chung TY

A 43-year-old man developed decreased vision in the right eye that had persisted for seven years. Under slit lamp examination, corneal clouding was noted with normal endothelium and ocular structure....
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Mutation Analysis of the TGFBI Gene in Consecutive Korean Patients With Corneal Dystrophies

Song JS, Lim DH, Chung ES, Chung TY, Ki CS

BACKGROUND: Mutations in the transforming growth factor beta-induced gene (TGFBI) are major causes of genetic corneal dystrophies (CDs), which can be grouped into TGFBI CDs. Although a few studies have...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Bietti Crystalline Retinopathy Confirmed by Mutation of CYP4V2 Gene in a Korean Patient

Park YJ, Hwang DJ, Seong MW, Park SS, Woo SJ

No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close

Go to Top

Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr