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This gene is associated with multiple cardiovascular, neurological and skeletal anomalies, including facial and ocular anomalies. The patient has been followed up periodically. Currently he presents a posterior embryotoxon in both eyes (<a class="elsevierStyleCrossRef" href="#fig0005">Fig.1</a>), with large centralized Schwalbe’s line displacement with iris adhesions, forming bridges. Therefore, Axenfeld-Rieger syndrome was diagnosed. 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Ophthalmology in images
Posterior embryotoxon as the initial ophthalmological sign of Axenfeld–Rieger syndrome
Embriotoxon posterior como primer signo oftalmológico del síndrome de Axenfeld-Rieger
D. Sweis Dahleh
, E. Jiménez Gañán, A. Serra Castanera
Corresponding author
Departamento de Oftalmología, Hospital San Joan de Déu, Barcelona, Spain