• A case of 22q11.2 deletion syndrome with Peters anomaly, congenital glaucoma, and heterozygous mutation in CYP1B1
• A case of childhood glaucoma with a combined partial monosomy 6p25 and partial trisomy 18p11 due to an unbalanced translocation
• A Case of WAGR Syndrome with Peters' Anomaly
• A compound heterozygous change found in Peters' anomaly
• A new autosomal dominant Peters' anomaly phenotype expanding the anterior segment dysgenesis spectrum
• A p.(Glu809Lys) Mutation in the WFS1 Gene Associated with Wolfram-like Syndrome: A Case Report
• Accuracy of Intraocular Pressure Measurement With the Icare Tonometer in Children
• Analysis of <em>CYP1B1</em> in pediatric and adult glaucoma and other ocular phenotypes
• Analysis of <em>CYP1B1</em> sequence alterations in patients with primary open-angle glaucoma of Saudi origin
• Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes
• Analysis of CYP1B1 sequence alterations in patients with primary open-angle glaucoma of Saudi origin
• Analysis of FOXD3 sequence variation in human ocular disease
• Analysis of long-term outcomes of penetrating keratoplasty for congenital corneal opacity
• Approach to childhood glaucoma: A review
• Atypical Peters plus syndrome with new associations
• Bilateral anterior segment dysgenesis with the presumed Peters' anomaly in a cat
• Bilateral lens subluxation associated with atopic eczema
• Case of novel PITX2 gene mutation associated with Peters' anomaly and persistent hyperplastic primary vitreous
• Causes of congenital corneal opacities and their management in a tertiary care center
• Chromosomal rearrangements and novel genes in disorders of eye development, cataract and glaucoma
• Clinical and diagnostic imaging profile of three anterior segment dysgenesis disorders presenting with infantile corneal opacities
• Clinical and Therapeutic Evaluation of the Ten Most Prevalent <em>CRB1</em> Mutations
• Clinical effects of pediatric penetrating keratoplasty for congenital corneal opacity
• Clinical profile and outcome of early surgery in neonatal-onset glaucoma presenting over a 5-year period
• Combined trabeculotomy and trabeculectomy as an initial procedure in uncomplicated congenital glaucoma
• Combined XEN and Baerveldt implant-principles and management of complications
• Complications and 2-year valve survival following Ahmed valve implantation during the first 2 years of life
• Congenital anterior segment ocular disorders: Genotype-phenotype correlations and emerging novel mechanisms
• Congenital aphakia in Peters' anomaly syndrome. A case report
• Congenital corneal opacities in a cornea referral practice
• Congenital glaucoma: future of vision and pressure. Results of an 11-year study
• Congenital hereditary endothelial dystrophy with progressive sensorineural deafness (Harboyan syndrome)
• Corneal transplants for the treatment of congenital corneal opacities
• Corrigendum: Optic neuropathy and congenital glaucoma associated with probable Zika virus infection in Venezuelan patients
• Cyp1b1 mediates periostin regulation of trabecular meshwork development by suppression of oxidative stress
• CYP1B1-related anterior segment developmental anomalies novel mutations for infantile glaucoma and von Hippel's ulcer revisited
• First observation of secondary childhood glaucoma in Coffin-Siris syndrome: a case report and literature review
• Forme fruste anterior segment dysgenesis
• General Treatment and Ophthalmic Management of Peters' Anomaly
• Genetic dissection of anterior segment dysgenesis caused by a <em>Col4a1</em> mutation in mouse
• Genetics of Congenital Corneal Opacification--Impact on Diagnosis and Treatment
• Genetics of the pediatric glaucomas
• Glaucoma Surgery in Anterior Segment Dysgeneses
• Histiocytoid cardiomyopathy and sudden death
• Image-guided femtosecond laser-assisted cataract surgery in Peters anomaly type 2
• Intestinal malrotation: another systemic anomaly associated with Peters' syndrome
• Keratoplasy for Peters anomaly (clinical case)
• Long-Term Clinical Course in Eyes With Peters Anomaly
• Long-Term Corneal Endothelial Cell Counts After Penetrating Keratoplasty in Infants
• Long-term visual prognosis in children after corneal transplant surgery for Peters anomaly type I
• Megalocornea
• Megalocornea
• Mendelian molecular genetics in glaucoma
• Microcephaly, bilateral corneal opacity and congenital lobar holoprosencephaly with subsequent development of a rhabdomyosarcoma in a patient exposed to prenatal radiation
• Mitomycin as adjunct chemotherapy with trabeculectomy in congenital and developmental glaucomas
• Molecular basis of Peters anomaly in Saudi Arabia
• Molecular genetics of primary congenital glaucoma in Brazil
• Mutation spectrum of the CYP1B1 gene for congenital glaucoma in the Japanese population
• Nasal dermoid sinus cyst: accidental coincidence or syndrome association?
• Novel CYP1B1 and known PAX6 mutations in anterior segment dysgenesis (ASD)
• Novel heterozygous variants in <em>PXDN</em> cause different anterior segment dysgenesis phenotypes in monozygotic twins
• Ocular manifestations in Peters' syndrome
• Optic neuropathy and congenital glaucoma associated with probable Zika virus infection in Venezuelan patients
• Optical iridectomy for corneal opacities in Peter's anomaly
• Optical sector iridectomy: an alternative to perforating keratoplasty in Peters' anomaly
• Outcomes of Ahmed Glaucoma Valve Revision in Pediatric Glaucoma
• Pathological and Immunohistochemical Alterations of the Cornea in Congenital Corneal Opacification Secondary to Primary Congenital Glaucoma and Peters Anomaly
• Persistent hyperplastic primary vitreous with myopia: a case study
• Peter's anomaly-A homeotic gene disorder
• Peters anomaly: An overview
• Peters' anomaly
• Peters' anomaly associated with protruding corneal pseudo staphyloma
• Peters' anomaly. A synopsis of surgical management and visual outcome
• Phenotype-genotype correlations and emerging pathways in ocular anterior segment dysgenesis
• Phenotypic heterogeneity of CYP1B1: mutations in a patient with Peters' anomaly
• Primary Congenital Glaucoma
• Primary Congenital Glaucoma
• Primary pediatric keratoplasty: indications and outcomes
• Prognostic factors of pediatric glaucoma: a retrospective study
• Risk and Prognostic Factors for Glaucoma Associated with Peters Anomaly
• Role of CYP1B1 in glaucoma
• Seeing clearly: the dominant and recessive nature of FOXE3 in eye developmental anomalies
• Should unilateral congenital corneal opacities in Peters' anomaly be grafted?
• Strabismus and amblyopia in bilateral Peters anomaly
• Surgical management of glaucoma in infants and children with Peters' anomaly: long-term structural and functional outcome
• Systemic Associations of Childhood Glaucoma: A Review
• Terminology of Peters' anomaly variants: Summary of histopathological findings in 6 corneas and detailed clinicopathological correlation in 2 cases
• The epidemiology of pediatric glaucoma: the Toronto experience
• The Ocular Neural Crest: Specification, Migration, and Then What?
• Three cases with unusual ophthalmic phenotypes of congenital aniridia
• Transplantation of congenitally opaque corneas
• Two adults with Rubinstein-Taybi syndrome with mild mental retardation, glaucoma, normal growth and skull circumference, and camptodactyly of third fingers
• Ultrasound biomicroscopy in infants with congenital corneal opacity and its correlations with clinical diagnosis and intraocular pressure
• Ultrasound evaluation of glaucoma drainage devices in children
• Unilateral buphthalmos, corneal staphyloma and corneal fistula caused by pathogenic variant in the PITX3 gene: a case report
• Unilateral Peters' anomaly complicated by a corneal tattoo
• Variable Anterior Segment Dysgenesis and Cardiac Anomalies Caused by a Novel Truncating Variant of FOXC1
• Variable Phenotype of Congenital Corneal Opacities in Biallelic CYP1B1 Pathogenic Variants
• Vitreoretinal dysplasia masquerading as Peters' anomaly
• XEN-augmented Baerveldt Implantation for Refractory Childhood Glaucoma: A Retrospective Case Series