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Achondroplasia With Congenital Onset Glaucoma, and Presumed Axenfeld-Rieger Anomaly.
We report the first case to our knowledge of a 1-week-old female infant with familial inherited achondroplasia associated with bilateral congenital onset glaucoma, posterior embryotoxon and iris hypoplasia suggestive of ocular Axenfeld-Rieger anomaly.