Unilateral posterior polymorphous corneal dystrophy due to a novel ZEB1 gene mutation in a Korean girl

Ophthalmic Genet. 2022 Oct;43(5):724-728. doi: 10.1080/13816810.2022.2106495. Epub 2022 Aug 31.

Authors

Chae Yeon Lee¹, Ja-Hyun Jang², Gyule Han¹, Tae-Young Chung¹, Dong Hui Lim^{1

3}

Affiliations

¹ Department of Ophthalmology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
² Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
³ Samsung Advanced Institute for Health Sciences and Technology, Sungkyunkwan University, Seoul, South Korea.

PMID: 36043701
DOI: 10.1080/13816810.2022.2106495

No abstract available

Publication types

Research Support, Non-U.S. Gov't
Letter

MeSH terms

Corneal Dystrophies, Hereditary* / diagnosis
Corneal Dystrophies, Hereditary* / genetics
Endothelium, Corneal
Female
Homeodomain Proteins / genetics
Humans
Mutation
Republic of Korea
Zinc Finger E-box-Binding Homeobox 1 / genetics

Substances

Homeodomain Proteins
ZEB1 protein, human
Zinc Finger E-box-Binding Homeobox 1

Supplementary concepts

Corneal Dystrophy, Posterior Polymorphous, 1