Disease: Microphthalmia cataract
- 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