• A case of childhood glaucoma with a combined partial monosomy 6p25 and partial trisomy 18p11 due to an unbalanced translocation
• A de novo mutation in <em>PITX2</em> underlies a unique form of Axenfeld-Rieger syndrome with corneal neovascularization and extensive proliferative vitreoretinopathy
• A donor twin discordant with Peters anomaly in a twin-twin transfusion syndrome case: a case report
• A mutation in DOP1B identified as a probable cause for autosomal recessive Peters anomaly in a consanguineous family
• A Novel Surgical Approach in the Management of Peters Anomaly With Glaucoma
• A rare case of type 1 unilateral 'peripheral' Peters' anomaly
• Activation of cryptic donor splice sites by non-coding and coding <em>PAX6</em> variants contributes to congenital aniridia
• Adams-Oliver syndrome: a case of bilateral progressive ischemic maculopathy
• Analysis of Graft Failure After Primary Penetrating Keratoplasty in Children With Peters Anomaly
• Analysis of long-term outcomes of penetrating keratoplasty for congenital corneal opacity
• Anomaly detection in mixed high dimensional molecular data
• Anomaly detection in mixed high-dimensional molecular data
• Anterior synechiae after penetrating keratoplasty in infants and children with Peters' anomaly
• Approach to childhood glaucoma: A review
• Atypical corneal clouding in mucopolysaccharidoses
• Atypical presentation of Cat Eye Syndrome in an infant with Peters anomaly and microphthalmia with cyst
• Bilateral Peters' anomaly, aniridia and Wilms tumour (WAGR syndrome) in monozygotic twins
• Bilateral primary hyperplastic persistent vitreous: report of two cases
• Case report of the rare Peters' anomaly complicated with Axenfeld-Rieger syndrome: A case report and brief review of the literature
• Causes of congenital corneal opacities and their management in a tertiary care center
• Clinical and diagnostic imaging profile of three anterior segment dysgenesis disorders presenting with infantile corneal opacities
• Clinical management of a rare Peters' anomaly-induced secondary childhood glaucoma: A case report
• Clinicopathologic Features and Treatment Characteristics of Congenital Corneal Opacity Infants and Children Aged 3 Years or Less: A Retrospective Single Institution Analysis
• CO(2) laser-assisted sclerectomy surgery and trabeculectomy combination therapy in Peters' anomaly-related glaucoma: a case report
• Congenital anterior segment ocular disorders: Genotype-phenotype correlations and emerging novel mechanisms
• Corneal Remodeling in Peters Anomaly
• Correlation of anterior segment optical coherence tomography and ultrasound biomicroscopy in congenital corneal opacity
• De Novo Missense Variants in WDR37 Cause a Severe Multisystemic Syndrome
• Distinct Roles of Histone Lysine Demethylases and Methyltransferases in Developmental Eye Disease
• Dominant variants in PRR12 result in unilateral or bilateral complex microphthalmia
• Endoscope-assisted scleral buckle procedure
• Extracellular vesicles: Emerging mediators of cell communication in gastrointestinal cancers exhibiting metabolic abnormalities
• First evidence of SOX2 mutations in Peters' anomaly: Lessons from molecular screening of 95 patients
• First observation of secondary childhood glaucoma in Coffin-Siris syndrome: a case report and literature review
• 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
• General Treatment and Ophthalmic Management of Peters' Anomaly
• Genetics Underlying the Interactions between Neural Crest Cells and Eye Development
• Glaucoma and Cornea Surgery Outcomes in Peters Anomaly
• Harboyan Syndrome
• Herbicide and Cytogenotoxic Activity of Inclusion Complexes of <em>Psidium gaudichaudianum</em> Leaf Essential Oil and <em>β</em>-Caryophyllene on 2-Hydroxypropyl-<em>β</em>-cyclodextrin
• Identification of a New Genetic Mutation Associated With Peters Anomaly
• Imaging Acute and Chronic Cardiac Complications of COVID-19 and after COVID-19 Vaccination
• Indications for intraoperative anterior segment optical coherence tomography in corneal surgery
• Integrated Intraoperative Optical Coherence Tomography for Pediatric Lamellar Corneal Transplant Surgery
• Intralobar sequestration associated with gastric enterogenous cyst: gastric lung!!
• Keratolenticular adhesion removal for type 2 Peters anomaly: a case report
• Keratoplasty in children : Indications and results
• Lacrimal drainage system involvement in Peters anomaly: clinical features and outcomes
• Long-term Experience and Visual Acuity Outcomes in Patients With Peters Anomaly
• Long-term experience and Visual Acuity outcomes in Peters Anomaly cases
• Long-Term Visual Outcomes and Clinical Course of Patients With Peters Anomaly
• Megalocornea
• New Phenotypic Feature in a Patient With a Rare Triplication of the 22q11.2 Region Presenting With Peters Anomaly, Congenital Heart Disease, and Global Developmental Delay: A Case Report and Literature Review
• Novel heterozygous variants in <em>PXDN</em> cause different anterior segment dysgenesis phenotypes in monozygotic twins
• Novel Loss of Function Variants in <em>CENPF</em> Including a Large Intragenic Deletion in Patients with Strømme Syndrome
• Novel Mutations in COL6A3 That Associated With Peters' Anomaly Caused Abnormal Intracellular Protein Retention and Decreased Cellular Resistance to Oxidative Stress
• Novel variants in CDH2 are associated with a new syndrome including Peters anomaly
• Ocular and brain imaging findings in Peters' anomaly: A case report and literature review
• Ocular Manifestations of Peters Plus-Like Syndrome in 8q21.11 Microdeletion Syndrome
• Ophthalmic involvement in PHACES syndrome: prevalence, spectrum of anomalies, and outcomes
• Outcomes of combined endoscopic vitrectomy and posteriorly placed glaucoma drainage devices in pediatric patients
• PAX8 Expression in the Crystalline Lens and Lens-Derived Lesions
• Penetrating Keratoplasty in Infants With Peters Anomaly: Visual and Graft Outcomes
• Persistent foetal vasculature masquerading as Peters anomaly
• Peter's anomaly-A homeotic gene disorder
• Peters Anomaly
• Peters Anomaly
• PETERS ANOMALY AND PETERS PLUS SYNDROME
• Peters Anomaly in Nail-Patella Syndrome: A Case Report and Clinico-Genetic Correlation
• Peters Anomaly in One Premature Twin Following Hydroxychloroquine Exposure During Pregnancy: A Case Report
• Peters Anomaly with Sequestered Lens in the Cornea
• Peters anomaly: A 5-year experience
• Peters anomaly: An overview
• Peters Anomaly: Novel Non-Invasive Alternatives to Penetrating Keratoplasty
• Peters plus syndrome and Chorioretinal findings associated with B3GLCT gene mutation - a case report
• Peters plus syndrome mutations affect the function and stability of human β1,3-glucosyltransferase
• Peters Plus syndrome: a recognizable clinical entity
• Phenotypic Spectrum of Peters Anomaly: Implications for Management
• Primary Congenital Glaucoma
• Quantitation of Pax-6 protein in ocular impression cytology samples using an electrochemiluminescence immunoassay
• Research progress of persistent hyperplastic primary vitreous with Peters anomaly
• Risk and Prognostic Factors for Glaucoma Associated with Peters Anomaly
• Scleral Lens Applications Focused on Korean Patients with Various Corneal Disorders
• Selective endothelial removal: A case series of a phase I/II surgical trial with long-term follow up
• Selective Endothelialectomy in Peters Anomaly: A Novel Surgical Technique and Its Clinical Outcomes in Children
• Short-Term Outcomes of Pediatric Keratoprosthesis With the Near-Complete Conjunctival Flap
• Sostdc1 is expressed in all major compartments of developing and adult mammalian eyes
• Spontaneous bilateral corneal perforation in a neonate: A case report
• Surgical approach in type II Peters anomaly - case report
• Swept-Source Anterior Segment OCT of Peters Anomaly Type 2
• T-cell Lymphoblastic Lymphoma in a Patient With Chromosome 8q21.11 Microdeletion
• Temporal Progression of Aortic Valve Pathogenesis in a Mouse Model of Osteogenesis Imperfecta
• Terminology of Peters' anomaly variants: Summary of histopathological findings in 6 corneas and detailed clinicopathological correlation in 2 cases
• The 2021 Congress of the International Society for Twin Studies: Twin Research at the Cutting Edge/Twin Research: Maternal Bonding with Twins; Twins with Peters Anomaly; Selective Termination in Dichorionic Twin Pairs; Neuropsychological Function in Twins
• The Ocular Neural Crest: Specification, Migration, and Then What?
• Ultrasound Biomicroscopy Detects Peters' Anomaly and Rieger's Anomaly in Infants
• Unilateral buphthalmos, corneal staphyloma and corneal fistula caused by pathogenic variant in the PITX3 gene: a case report
• Variable Phenotype of Congenital Corneal Opacities in Biallelic CYP1B1 Pathogenic Variants
• Visual Outcomes in Pediatric Patients with Peters Anomaly
• XEN-augmented Baerveldt Implantation for Refractory Childhood Glaucoma: A Retrospective Case Series