Congenital Cataract | List of Frontiers open access articles

Case Report

Published on 10 Feb 2022

Case Report: A Novel Mutation in the CRYGD Gene Causing Congenital Cataract Associated with Nystagmus in a Chinese Family

in Genetics of Common and Rare Diseases

Yunxia Gao
Xiang Ren
Xiangyu Fu
Yu Lin
Lirong Xiao
Xiaoyue Wang
Naihong Yan
Ming Zhang

Frontiers in Genetics

doi 10.3389/fgene.2022.824550

3,444 views
3 citations

Original Research

Published on 16 Feb 2024

Characteristic cytokine profile of the aqueous humor in eyes with congenital cataract and pre-existing posterior capsule dysfunction

in Ophthalmology

Yinying Zhao
Qihui Zhao
Hongfang Zhang
Zhewen Zhang
Dandan Wang
Zhangliang Li
Xixia Ding
Yune Zhao

Frontiers in Medicine

doi 10.3389/fmed.2024.1301588

2,206 views
1 citation

Case Report

Published on 27 May 2022

Case Report: A de novo Variant of CRYGC Gene Associated With Congenital Cataract and Microphthalmia

in Genetics of Common and Rare Diseases

Yu Peng
Yu Zheng
Zifeng Deng
Shuju Zhang
Yilan Tan
Zhengmao Hu
Lijuan Tao
Yulin Luo

Frontiers in Genetics

doi 10.3389/fgene.2022.866246

3,063 views
3 citations

Case Report

Published on 01 Jul 2022

Case Report: Combined Cataract Surgery and Minimally Invasive Glaucoma Surgery Provide an Alternative Treatment Approach for Lowe Syndrome

in Ophthalmology

Chen Wang
Wenzhe Zhang
Leyi Wang
Wenhui Liu
Hui Guo

Frontiers in Medicine

doi 10.3389/fmed.2022.913229

3,613 views
1 citation

Original Research

Published on 21 Feb 2023

Capsulotomy opening diameter outcomes in aphakic eyes after primary congenital cataract removal and its association

in Pediatric Surgery

Qihui Zhao
Pingjun Chang
Yinying Zhao
Dandan Wang
Yune Zhao

Frontiers in Pediatrics

doi 10.3389/fped.2023.1062144

2,681 views

Case Report

Published on 24 Jul 2025

Case Report: A family of congenital cataract caused by a novel mutation in the CRYGC gene c.52G>A

in Ophthalmology

Shuying Ma
Yao Lu
Xiao Shao
Qingyan Liu
Xin Yin
Min Xue

Frontiers in Medicine

doi 10.3389/fmed.2025.1624834

2,693 views
1 citation

Case Report

Published on 29 Feb 2024

Case report: Whole exome sequencing identified a novel mutation (p.Y301H) of MAF in a Chinese family with congenital cataracts

in Ophthalmology

Zhao-Jing Lin
Jie-Yi Long
Juan Li
Fang-Na Wang
Wei Chu
Lei Zhu
Ya-Li Li
Liang-Liang Fan

Frontiers in Medicine

doi 10.3389/fmed.2024.1332992

2,769 views
1 citation

Review

Published on 26 Sep 2025

Insights and decision-making on surgical triggers of glaucoma-related complications in congenital cataract surgery: a clinical review

in Ophthalmology

Bin Lin
Wei Fan
Dong-kan Li

Frontiers in Medicine

doi 10.3389/fmed.2025.1622410

2,187 views

Original Research

Published on 21 Apr 2022

Identification of a New Mutation p.P88L in Connexin 50 Associated with Dominant Congenital Cataract

in Molecular and Cellular Pathology

Aixia Jin
Qingqing Zhao
Shuting Liu
Zi-bing Jin
Shuyan Li
Mengqing Xiang
Mingbing Zeng
Kangxin Jin

Frontiers in Cell and Developmental Biology

doi 10.3389/fcell.2022.794837

3,987 views
9 citations

Original Research

Published on 05 Sep 2025

Epidemiological characteristics, distribution of axial length, and prevalence of ocular abnormalities associated with congenital cataract in Northwest China: a 16-year cross-sectional study (2008–2023)

in Ophthalmology

Mengmei He
Min Gong
Guorui Dou
Jian Zhou
Xu Hou

Frontiers in Medicine

doi 10.3389/fmed.2025.1617601

1,980 views

Case Report

Published on 30 Jan 2026

Case Report: Sengers syndrome caused by a novel 7.6 kb AGK deletion misdiagnosed as isolated congenital cataract

in Genetics of Common and Rare Diseases

Xingwang Gong
Yue Liu
Hui Liang

Frontiers in Pediatrics

doi 10.3389/fped.2026.1714952

366 views

Original Research

Published on 03 Jun 2025

Online platform vs. doctors: a comparative exploration of congenital cataract patient education from virtual to reality

in Medicine and Public Health

Xuanqiao Lin
Lifang Bai
Xiaohuan Zhao
Lei Cai
Jin Yang

Frontiers in Artificial Intelligence

doi 10.3389/frai.2025.1548385

3,301 views

Original Research

Published on 02 Dec 2022

Molecular diagnosis of autosomal dominant congenital cataract in two families from North India reveals a novel and a known variant in GJA8 and GJA3

in Genetics of Common and Rare Diseases

Vanita Vanita
Shiwali Goyal
Shailja Tibrewal
Suma Ganesh

Frontiers in Pediatrics

doi 10.3389/fped.2022.1003909

2,552 views
3 citations

Original Research

Published on 02 Dec 2021

Defect of LSS Disrupts Lens Development in Cataractogenesis

in Molecular and Cellular Pathology

Minglei Zhao
Tingfang Mei
Bizhi Shang
Bin Zou
Qing Lian
Wenchang Xu
Keling Wu
Yuhua Lai
Chujun Liu
Lai Wei

Frontiers in Cell and Developmental Biology

doi 10.3389/fcell.2021.788422

8,054 views
16 citations

Case Report

Published on 16 Sep 2021

Case Report: A Novel Missense Variant in the SIPA1L3 Gene Associated With Cataracts in a Chinese Family

in Genetics of Common and Rare Diseases

Duo Yang
Haiyan Zhou
Jiwu Lin
Shuangxi Zhao
Hao Zhou
Zhaochu Yin
Bin Ni
Yong Chen
Wanqin Xie

Frontiers in Genetics

doi 10.3389/fgene.2021.715599

3,002 views

Original Research

Published on 14 Apr 2021

Reduced Functional Connectivity in Children With Congenital Cataracts Using Resting-State Electroencephalography Measurement

in Perception Science

Wan Chen
Liping Lan
Wei Xiao
Jiahong Li
Jiahao Liu
Fei Zhao
Chang-Dong Wang
Yiqing Zheng
Weirong Chen
Yuexin Cai

Frontiers in Neuroscience

doi 10.3389/fnins.2021.657865

4,600 views
1 citation

Articles

Case Report: A Novel Mutation in the CRYGD Gene Causing Congenital Cataract Associated with Nystagmus in a Chinese Family

Characteristic cytokine profile of the aqueous humor in eyes with congenital cataract and pre-existing posterior capsule dysfunction

Case Report: A de novo Variant of CRYGC Gene Associated With Congenital Cataract and Microphthalmia

Case Report: Combined Cataract Surgery and Minimally Invasive Glaucoma Surgery Provide an Alternative Treatment Approach for Lowe Syndrome

Capsulotomy opening diameter outcomes in aphakic eyes after primary congenital cataract removal and its association

Case Report: A family of congenital cataract caused by a novel mutation in the CRYGC gene c.52G>A

Case report: Whole exome sequencing identified a novel mutation (p.Y301H) of MAF in a Chinese family with congenital cataracts

Insights and decision-making on surgical triggers of glaucoma-related complications in congenital cataract surgery: a clinical review

Identification of a New Mutation p.P88L in Connexin 50 Associated with Dominant Congenital Cataract

Epidemiological characteristics, distribution of axial length, and prevalence of ocular abnormalities associated with congenital cataract in Northwest China: a 16-year cross-sectional study (2008–2023)

Case Report: Sengers syndrome caused by a novel 7.6 kb AGK deletion misdiagnosed as isolated congenital cataract

Online platform vs. doctors: a comparative exploration of congenital cataract patient education from virtual to reality

Molecular diagnosis of autosomal dominant congenital cataract in two families from North India reveals a novel and a known variant in GJA8 and GJA3

Defect of LSS Disrupts Lens Development in Cataractogenesis

Case Report: A Novel Missense Variant in the SIPA1L3 Gene Associated With Cataracts in a Chinese Family

Reduced Functional Connectivity in Children With Congenital Cataracts Using Resting-State Electroencephalography Measurement