• 'Ɛ' sign: a clinical clue to the diagnosis of microspherophakia
• <em>PAX6</em> disease models for aniridia
• A case of Axenfeld-Rieger syndrome (ARS) with asymmetric ocular phenotypes and left glaucomatous optic atrophy
• A large deletion spanning <em>PITX2</em> and <em>PANCR</em> in a Chinese family with Axenfeld-Rieger syndrome
• A novel frameshift mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome using targeted exome sequencing
• A novel missense mutation of FOXC1 in an Axenfeld-Rieger syndrome patient with a congenital atrial septal defect and sublingual cyst: a case report and literature review
• A novel mutation in the aspartate beta-hydroxylase (<em>ASPH</em>) gene is associated with a rare form of Traboulsi syndrome
• A PITX2 splice-site mutation in a family with Axenfeld-Rieger syndrome leads to decreased expression of nuclear PITX2 protein
• A rare presentation of bilateral dislocated lens in a patient with isolated microspherophakia
• A safer alternative approach to penetrating keratoplasty in opaque corneas
• A systematic approach to the management of microspherophakia
• A Wide Spectrum of Ocular Manifestations Signify Patients with Systemic Sclerosis
• Acute iris toxicity following bilateral gel stent implantation with mitomycin-C and intracameral moxifloxacin January consultation #1
• Analysis of genotype-phenotype correlation in Walker-Warburg syndrome with a novel <em>CRPPA</em> mutation in different clinical manifestations
• Aniridic Fibrosis Syndrome
• Aniridic glaucoma: An update
• Aniridic glaucoma: An update
• Anterior megalophthalmos in sisters with Witteveen-Kolk syndrome
• Anterior segment dysgenesis and secondary glaucoma in Goldenhar syndrome
• Atypical presentations of non-familial anterior megalophthalmos: a rare disease
• Automated Iris Segmentation from Anterior Segment OCT Images with Occludable Angles via Local Phase Tensor
• Axenfeld-Rieger syndrome combined with a foveal anomaly in a three-generation family: a case report
• Axenfeld-Rieger syndrome combined with ectropion uveae and pigment dispersion syndrome: A case report
• Axenfeld-Rieger syndrome in monozygotic twin brothers: Case report
• Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma
• Biallelic variants in <em>CPAMD8</em> are associated with primary open-angle glaucoma and primary angle-closure glaucoma
• Case of Pierson syndrome presented with hyphema,vitrous haemorrhage and subsequent neovascular glaucoma
• Chromosome 6p25 deletion syndrome: A case report and review of ophthalmic features
• Clinical and molecular aspects of congenital aniridia - A review of current concepts
• Clinical and pathological characterization of ophthalmic disease in a canine model of mucopolysaccharidosis type I
• Clinical Manifestations and Long-term Outcomes of Endothelial Keratoplasty in Patients with Proven VZV-related Endothelial Decompensation
• Comparison of Anterior Segment Abnormalities in Individuals With FOXC1 and PITX2 Variants
• Complicated microspherophakia in a paediatric patient
• Complications of a congenital iris cyst in a newborn
• Complications of Cosmetic Artificial Iris Implantation and Post Explantation Outcomes
• Compound heterozygous mutations in the LTBP2 gene associated with microspherophakia in a Chinese patient: a case report and literature review
• Congenital aniridia - A comprehensive review of clinical features and therapeutic approaches
• Congenital aniridia - Hungarian data of a spectrum disease
• Congenital ciliary body cysts causing lens abnormalities and secondary angle closure glaucoma in a child
• CPAMD8 loss-of-function underlies non-dominant congenital glaucoma with variable anterior segment dysgenesis and abnormal extracellular matrix
• Detection of a novel PAX6 variant in a Chinese family with multiple ocular abnormalities
• Diagnosis and treatment of microspherophakia
• Diversity of clinical phenotypes in a cohort of Han Chinese patients with <em>PAX6</em> variants
• Dry-Lensectomy Assisted Lensectomy in the Management for End-Stage Familial Exudative Vitreoretinopathy Complicated With Anterior Segment Abnormalities
• Ectropion Uveae in neurofibromatosis type 1: a new manifestation
• Efficacy of Combined Phacoemulsification and Goniosynechialysis in Primary Angle Closure Disease With Different Degrees of Peripheral Anterior Synechiae
• Exome sequencing and functional studies in zebrafish identify WDR8 as the causative gene for isolated Microspherophakia in Indian families
• Eye pain and blurred vision as main complaints in a new case with MDPL syndrome
• Formulation and Stability of Ataluren Eye Drop Oily Solution for Aniridia
• Fourteen-Year Outcome of Angle-Closure Prevention with Laser Iridotomy in the Zhongshan Angle-Closure Prevention Study: Extended Follow-up of a Randomized Controlled Trial
• FOXC1 variant in a family with anterior segment dysgenesis and normal-tension glaucoma
• Gallic acid and myricetin-rich Labisia pumila extract mitigated multiple diabetic eye disorders in rats
• Genetic mapping of autosomal recessive microspherophakia to chromosome 14q24.3 in a consanguineous Pakistani family and screening of exon 36 of LTBP2 gene
• High Iris Insertion in Axenfeld-Rieger Syndrome
• Integrated Intraoperative Optical Coherence Tomography in Pediatric Glaucoma Surgery
• Iridocorneal Dysgenesis
• Iridocorneal Endothelial Syndrome with Coexisting Macular Edema and Neurosensory Detachment: An Unusual Case Report
• Iridocorneal Endothelial Syndrome: Case Report of Essential Progressive Iris Atrophy
• Iridoschisis-A Systematic Review
• Iris abnormalities may influence the efficacy and filtration strategies of Posner-Schlossman syndrome: a retrospective study involving trabeculectomy, ExPRESS and Ahmed valve implants
• Isolated microspherophakia with retinitis pigmentosa
• Kissing microvitreoretinal blade technique: A novel approach for safe and effective endocapsular lens aspiration in microspherophakia
• Lens Coloboma: A Rare Association of Congenital Rubella Syndrome
• Lens in Primary Congenital Glaucoma Eyes Treated by Combined Angle and Filtering Surgery
• Lenticular corona: Aura of the microspherophakic lens
• Longitudinal genotype-phenotype analysis in 86 patients with PAX6-related aniridia
• Macular involvement in congenital aniridia
• Macular involvement in congenital aniridia
• Megalocornea
• Microphthalmia and anterior segment dysgenesis due to a double gene variant in <em>GJA8</em> and <em>CRYGC</em>
• Microspherophakia with Novel Gene Mutations in a Young Girl
• Morphology, family history, and age at diagnosis of 26 patients with Axenfeld-Rieger syndrome and glaucoma or ocular hypertension
• Morphometric analysis of the lens in human aniridia and mouse Small eye
• Mutational analysis and genotype-phenotype correlations in southern Indian patients with sporadic and familial aniridia
• Nail-Patella Syndrome: Optical Coherence Tomography Angiography Findings
• National protocol for diagnosis and care of congenital aniridia: Summary for the attending physician
• Neonatal Onset Glaucoma in a Case with Gorlin-Goltz Syndrome: An Unusual Association
• Neurofibromatosis type 1 initially presented with glaucoma in the Department of Ophthalmology: a case report
• Novel double-flanged technique for managing Marfan syndrome and microspherophakia
• Novel heterozygous variants in <em>PXDN</em> cause different anterior segment dysgenesis phenotypes in monozygotic twins
• Occult cause of uveitis-glaucoma-hyphema syndrome diagnosed during treatment with endocyclophotocoagulation (ECP)
• Ocular hypertension in Axenfeld-Rieger Syndrome
• Ophthalmological Manifestations of Axenfeld-Rieger Syndrome: Current Perspectives
• Optic Disc Pit Maculopathy - Case Series, Clinical Approach, and Management
• Optic Nerve Aplasia
• Pre- and Post-Surgical Microspherophakia Anterior-Segment OCT
• Primary Congenital Glaucoma
• Qualitative ultrasound biomicroscopy in glaucoma
• Retropupillary iris claw lens versus Gore-Tex assisted scleral fixated intraocular lens in children with large lens subluxations
• Spectrum of Genetic Variants Associated with Anterior Segment Dysgenesis in South Florida
• Surgical Management of Iris Bombe in Muscle-Eye-Brain Disease
• The Contribution of Anterior Segment Abnormalities to Changes in Intraocular Pressure in the DBA/2J Mouse Model of Glaucoma: DBA/2J-<em>Gpnmb</em> ⁺/SjJ Mice as Critical Controls
• The risk of glaucoma associated with phacomatosis cesioflammea and phacomatosis cesioflammeo-marmorata
• Traboulsi Syndrome in Pakistan
• Traboulsi syndrome without features of Marfan syndrome caused by a novel homozygous <em>ASPH</em> variant associated with a heterozygous <em>FBN1</em> variant
• Transgenic Overexpression of Myocilin Leads to Variable Ocular Anterior Segment and Retinal Alterations Associated with Extracellular Matrix Abnormalities in Adult Zebrafish
• Untargeted metabolomics in the aqueous humor reveals the involvement of TAAR pathway in glaucoma
• Variable Anterior Segment Dysgenesis and Cardiac Anomalies Caused by a Novel Truncating Variant of FOXC1
• Visual quality observation of clear lens extraction by ultrasonic phacoemulsification and intraocular lens implantation in a child with microspherophakia: A case report
• When the savior becomes a demon: Silicon oil synechia-induced glaucoma