Disease: Peters congenital glaucoma
- 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 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
- Keratoplasty in newborns with Peters' anomaly
- 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