Disease: Total Congenital Cataracts
- A comparative study of rigid gas permeable corneal contact lenses versus frame glasses for refractive correction of postoperative aphakic eyes after congenital cataract surgery in infants and children
- Analysis of disease composition and primary surgical procedures in pediatric secondary glaucoma inpatients: a single-center study
- Aqueous Humor Cytokine Profile in Primary Congenital Glaucoma
- Biomarkers of Pediatric Cataracts: A Proteomics Analysis of Aqueous Fluid
- Breed predispositions to congenital and juvenile cataracts in horses at two academic institutions
- Childhood glaucoma profile in a Southwestern Ethiopia tertiary care center: a retrospective study
- Childhood glaucoma profile in a tertiary centre in Egypt according to the childhood glaucoma research network classification
- Clinical and demographic profile of pediatric cataracts among Omani children presenting to a tertiary eye care center, Oman
- Combined trabeculotomy-trabeculectomy for glaucoma after congenital cataract surgery: long-term results
- Congenital Cataracts with Thin Lenses (Leptophakia) in Children: Morphology and Surgical Outcomes
- Congenital coralliform cataract is the predominant consequence of a recurrent mutation in the CRYGD gene
- Contact lenses in paediatric aphakia in the Netherlands; A multicentre retrospective chart study
- Early Diagnosis of Syndromic Congenital Cataracts in a Large Cohort of Congenital Cataracts
- Evaluation of Genetic Testing in a Cohort of Diverse Pediatric Patients in the United States with Congenital Cataracts
- First Case Report of Developmental Bilateral Cataract with a Novel Mutation in the <em>ZEB2</em> Gene Observed in Mowat-Wilson Syndrome
- Functional Vision of Pseudophakic Children Attending a Pediatric Ophthalmology Clinic in Southwest Nigeria
- Genotypic-Phenotypic Correlations of Hereditary Hyperferritinemia-Cataract Syndrome: Case Series of Three Brazilian Families
- Hallermann-Streiff Syndrome in Concordant Monozygotic Twins With Congenital Cataracts, Exudative Retinal Detachments, and One Case of Corneal Perforation Requiring Keratoplasty
- Identification of a Missense Mutation in <em>GJA8</em> Gene in an Iranian Family with Autosomal Dominant Congenital Cataract
- Identification of a Missense Mutation in GJA8 Gene in an Iranian Family with Autosomal Dominant Congenital Cataract
- Incidence Rate of Secondary Glaucoma Following Congenital Cataract Surgery: An In-Depth Systematic Review and Meta-Analysis
- Intraocular lens power calculation formulas: a scientometric analysis
- Lens Coloboma: A Rare Association of Congenital Rubella Syndrome
- Metabolomic Profiling of the Aqueous Humor in Patients with Pediatric Cataract
- Novel <em>CRYGC</em> Mutation in Conserved Ultraviolet-Protective Tryptophan (p.Trp131Arg) Is Linked to Autosomal Dominant Congenital Cataract
- Novel CRYGC Mutation in Conserved Ultraviolet-Protective Tryptophan (p.Trp131Arg) Is Linked to Autosomal Dominant Congenital Cataract
- Outcomes for non-treatment-requiring infants evaluated for retinopathy of prematurity
- Parent-of-Origin Effect on the Age at Symptom Onset in Myotonic Dystrophy Type 2
- Predictive Factors of Complications and Visual Outcomes after Pediatric Cataract Surgery: A Single Referral Center Study from Turkiye
- Predictive factors of occult cystobiliary fistulas during conservative treatment of hepatic hydatid cyst: a prospective study
- Predictors of Glaucoma After Pediatric Cataract Surgery
- Prevalence and prenatal diagnosis of congenital eye anomalies: A population-based study
- Prevalence of Glaucoma Following Paediatric Cataract Surgery in an Australian Tertiary Referral Centre
- Profile of Newly Diagnosed Childhood Glaucoma in India: ICGS 1
- Profile of Newly Diagnosed Childhood Glaucoma in India: Indian Childhood Glaucoma Study (ICGS) Group 1
- Retinal microvascular changes in unilateral functional amblyopia detected by oct-angiography and follow-up during treatment
- Retrospective analysis of low vision assistive products - A 6-year review
- Ribonuclease inhibitor 1 (RNH1) deficiency cause congenital cataracts and global developmental delay with infection-induced psychomotor regression and anemia
- Single-center experience of congenital disorders of glycosylation syndrome screening in Tunisia: A retrospective study over a 15-year period (2007-2021)
- Surgical management of complicated Descemet's membrane detachment in corneas without prior endothelial keratoplasty
- Surgical Outcomes of Lensectomy-Vitrectomy with Primary Intraocular Lens Implantation in Children with Bilateral Congenital Cataracts
- Ten-year refractive and visual outcomes of intraocular lens implantation in infants with congenital cataract