Expanded Phenotype of PAX2-Related Papillorenal Syndrome: A Case Featuring FSGS, Atypical Retinopathy, Cerebellar Hypoplasia, and ADHD. [PDF]
Sultana N, Mamun AA, Begum A.
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A novel mutation in the human RAX gene in patients with microphthalmia and coloboma: A case report and literature review. [PDF]
Li Z, Ke S, Wan W, Sun J, Hu K, Li C.
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Case Report: Sturge-Weber syndrome with contralateral morning glory syndrome. [PDF]
Wang L +7 more
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Refractive Error Correction With Glasses in Congenital Ocular Fundus Anomalies: A Retrospective Series of 18 Children With Different Disease Entities Followed Up for More Than 10 Years. [PDF]
Matsuo T.
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Autologous Tenon's Capsule Graft for Recurrent Retinal Detachment Associated with a Cavitary Optic Disc Anomaly following Failed Amniotic Membrane Grafting. [PDF]
Mohammadi N +2 more
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Amniotic membrane placement without endotamponade for optic nerve coloboma with extensive serous retinal detachment in papillorenal syndrome: A case report. [PDF]
Lucchini S +5 more
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Morning Glory Disc Anomaly With Ipsilateral Carotid Vasculopathy: MRI Characteristics and Clinical Implications. [PDF]
Radder N, Radder S.
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Ocular Findings in Siblings With Alagille Syndrome: A Report of Two Cases. [PDF]
Murati Calderon RA +2 more
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Variants in the CxxC domain of the epigenetic regulator KDM2B support its role in developmental eye anomalies. [PDF]
Ceroni F +12 more
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