• A Boy with Sandestig-Stefanova Syndrome and Genital Abnormalities
• A Comparative Study on the Accuracy of IOL Calculation Formulas in Nanophthalmos and Relative Anterior Microphthalmos
• A Cross-sectional Analysis of 556 Eyes Entering the Homburg Aniridia Centre
• A Fetus with Congenital Microcephaly, Microphthalmia and Cataract Was Detected with Biallelic Variants in the OCLN Gene: A Case Report
• A New Case and Comprehensive Review of the Ophthalmic Manifestations of 172 Individuals With Branchio-Oculo-Facial Syndrome
• A novel deletion mutation in the BCOR gene is associated with oculo-facio-cardio-dental syndrome: a case report
• A Novel Mutation in <em>CRYGC</em> Mutation Associated with Autosomal Dominant Congenital Cataracts and Microcornea
• A Novel Mutation in CRYGC Mutation Associated with Autosomal Dominant Congenital Cataracts and Microcornea
• A rare genotype of biallelic mosaic variants in BCOR gene causing a bilateral ocular anterior segment dysgenesis and cataracts
• A report on a series of nanophthalmos with histopathology and immunohistochemistry analyses using light microscopy
• A Review of Human Ocular RNA Virus Infections Excluding Coronavirus, Human T-Cell Lymphotropic Virus, and Arboviruses
• An Extremely Rare Case of Bonneau Syndrome with Novel Cardiac and Eye Manifestations
• Association of variants in GJA8 with familial acorea-microphthalmia-cataract syndrome
• Bi-allelic mutation of CTNNB1 causes a severe form of syndromic microphthalmia, persistent foetal vasculature and vitreoretinal dysplasia
• Bilateral anterior segment dysgenesis and persistent fetal vasculature associated with terminal 10q26 deletion
• Case Report: A <em>de novo</em> Variant of <em>CRYGC</em> Gene Associated With Congenital Cataract and Microphthalmia
• Case Report: A de novo Variant of CRYGC Gene Associated With Congenital Cataract and Microphthalmia
• Case report: Expansion of phenotypic and genotypic data in <em>TENM3</em>-related syndrome: Report of two cases
• Cataract surgery and the small eye: relative anterior microphthalmos, high hyperopia and nanophthalmos
• Cataract surgery in colobomatous eyes with advanced cataract
• Characterization of a Novel Gja8 (Cx50) Mutation in a New Cataract Rat Model
• Clinical and genetic analysis further delineates the phenotypic spectrum of ALDH1A3-related anophthalmia and microphthalmia
• Clinical characteristics and ophthalmic management of a rare disease cohort of patients with trisomy 13
• Clinical update in nanophthalmos: Features, diseases and complications associated
• Commentary: Short eyes and bigger challenges - Growing evidence in the management of pediatric nanophthalmos
• Commercial Gene Panels for Congenital Anterior Segment Anomalies: Are They All the Same?
• Comparing Gene Panels for Non-Retinal Indications: A Systematic Review
• Congenital ocular toxoplasmosis with torpedo maculopathy and retinopathy of prematurity in a premature baby
• Correlated color temperature is not a suitable proxy for the biological potency of light
• Couching of cataractous lens in microphthalmic eyes with irido-fundal coloboma: revisiting the historical technique
• Dandy-Walker Variant Associated with Bilateral Congenital Cataract
• Design and Outcomes of a Novel Multidisciplinary Ophthalmic Genetics Clinic
• Dysregulation of Autophagy Occurs During Congenital Cataract Development in betaA3deltaG91 Mice
• Embryology, Eye Malformations
• Embryology, Eye Malformations
• EPHA2 biallelic disruption causes syndromic complex microphthalmia with iris hypoplasia
• Exome sequencing identifies a novel pathogenic variant in RAB3GAP1 causing Warburg Micro syndrome in a Pakistani family
• Expanding the phenotypic and allelic spectrum of SMG8: Clinical observations reveal overlap with SMG9-associated disease trait
• Fetal eye ultrasound: Normal anatomy, abnormal findings, and clinical impact
• Findings of ocular examinations in healthy full-term newborns
• First Clinical Report of Two <em>RAB3GAP1</em> Pathogenic Variant in Warburg Micro Syndrome
• First implication of MIP in bilateral microphthalmia with persistent fetal vasculature
• First Report of Mexican Patients with <em>PACS1</em>-Related Neurodevelopmental Disorder and Review of the <em>PACS1</em>-, <em>PACS2</em>-, and <em>WDR37</em>-Related Ophthalmological Manifestations
• Foveal Hypoplasia Related to Congenital Rubella
• Foveal photoreceptor atrophy, persistent fetal vasculature, congenital cataracts, and microphthalmia in a pediatric patient with BCOR-associated oculo-facio-cardio-dental (OFCD) syndrome
• Genome sequencing in congenital cataracts improves diagnostic yield
• Hallermann-Streiff Syndrome and Psychosis: A Case Report
• Hallermann-Streiff syndrome diagnosed in the seventh decade of life
• HSP90beta prevents aging-related cataract formation through regulation of the charged multivesicular body protein (CHMP4B) and p53
• HSP90β prevents aging-related cataract formation through regulation of the charged multivesicular body protein (CHMP4B) and p53
• Identification and functional analysis of two GJA8 variants in Chinese families with eye anomalies
• Identification of a novel microdeletion causative of Nance-Horan syndrome
• Impacts of High Environmental Temperatures on Congenital Anomalies: A Systematic Review
• Insight into small eyes: a practical description from phenotypes presentations to the management
• Juvenile ocular abnormalities in a litter of black-footed ferrets
• Knockout of miR-184 in zebrafish leads to ocular abnormalities by elevating p21 levels
• Late-onset glaucoma following congenital cataract surgery: Occurrence, visual acuity and risk factors: A 37-year longitudinal follow-up
• Lens Coloboma: A Rare Association of Congenital Rubella Syndrome
• Longitudinal study of microphthalmia in connexin 50 knockout mice using spectral-domain optical coherence tomography
• Macrophthalmos mimics microphthalmos in an 8-month-old Great Swiss Mountain Dog
• Microphthalmia and anterior segment dysgenesis due to a double gene variant in <em>GJA8</em> and <em>CRYGC</em>
• Microphthalmia and anterior segment dysgenesis due to a double gene variant in GJA8 and CRYGC
• Microphthalmia and congenital cataract in two patients with Stickler syndrome type II: a case report
• Multiple pancreatic neuroendocrine tumors in OFCD syndrome caused by somatic BCOR mosaicism
• Myopic Posterior Persistent Fetal Vasculature: A Rare Presentation
• Nance-Horan Syndrome: characterization of dental, clinical and molecular features in three new families
• New ocular findings in a patient with a novel pathogenic variant in the FBXO11 gene
• Non-typical persistent hyperplastic primary vitreous: a rare case report and review of the literature
• Nonsense-mediated mRNA decay affects hyperactive root formation in oculo-facio-cardio-dental syndrome via up-frameshift protein 1
• Novel <em>RAB3GAP1</em> Mutation in the First Tunisian Family With Warburg Micro Syndrome
• Novel <em>SIX6</em> mutations cause recessively inherited congenital cataract, microcornea, and corneal opacification with or without coloboma and microphthalmia
• Novel Mutation in CRYBB3 Causing Pediatric Cataract and Microphthalmia
• Novel SIX6 mutations cause recessively inherited congenital cataract, microcornea, and corneal opacification with or without coloboma and microphthalmia
• Ocular manifestations of CHARGE syndrome in a pediatric cohort with genotype/phenotype analysis
• Ocular manifestations of congenital anomalies of the kidney and urinary tract (CAKUT)
• Ocular severe involvement in oculofaciocardiodental syndrome: Description of a case series
• Oculo-facio-cardio-dental syndrome caused by <em>BCOR</em> gene mutations: a case report
• Outcomes of surgical treatment of congenital cataract with microphthalmia in infancy
• P02-A121 Precut DSAEK stored in an active storage machine: feasibility study
• PHACE(S) Syndrome with Ocular Involvements and No Periocular Hemangioma
• Posterior microphthalmos with exudative retinal detachment after piggyback intraocular lens implantation: A case report
• Postoperative complications and axial length growth after bilateral congenital cataract surgery: eyes with microphthalmos compared to a comparison group
• Prenatal and Postnatal Ocular Abnormalities Following Congenital Zika Virus Infections: A Systematic Review
• Prevalence and prenatal diagnosis of congenital eye anomalies: A population-based study
• Ptosis Correction
• Ptosis Correction
• Subluxated cataractous lens and high myopia: An uncommon association in an achondroplasia child
• The association of nausea and vomiting of pregnancy, its treatments, and select birth defects: Findings from the National Birth Defect Prevention Study
• The effect of implantable collamer Lens V4c on ocular biometric measurements and intraocular lens power calculation based on Pentacam-AXL and IOLMaster 500
• The impact of conditional cash transfers for HIV prevention on peer relationships: perspectives from female recipients and non-recipients in HPTN 068
• The Prevalence of Cataract in Children
• The RhoGAP-myosin Myo9b regulates ocular lens pit morphogenesis
• Therapeutic Strategies in 103 Children with Congenital Microphthalmos
• Treatment of Nanophthalmos Cataracts: Surgery and Complications
• Understanding the effect of correlated colour temperatures on spatio-chromatic properties of natural images
• Unilateral buphthalmos, corneal staphyloma and corneal fistula caused by pathogenic variant in the PITX3 gene: a case report
• Variants of BEST1 and CRYBB2 cause a complex ocular phenotype comprising microphthalmia, microcornea, cataract, and vitelliform macular dystrophy: case report
• Vision Development in a Hallermann-Streiff Case with Bilateral Severe Microphthalmia, Cataract and Extensive Retinal Folds
• Whole-Exome Sequencing and Copy Number Analysis in a Patient with Warburg Micro Syndrome
• Znhit1 Regulates p21Cip1 to Control Mouse Lens Differentiation