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Last Updated : 05/19/2022

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Found 11 publications

Case report of the rare Peters' anomaly complicated with Axenfeld-Rieger syndrome: A case report and brief review of the literature.

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.

Laser corepraxy in mesodermal iris dysgenesis (Axenfeld-Rieger syndrome) (case report).

Axenfeld-Rieger syndrome combined with a foveal anomaly in a three-generation family: a case report.

The Axenfeld-Rieger Syndrome Gene FOXC1 Contributes to Left-Right Patterning.

Loss of FOXC1 contributes to the corneal epithelial fate switch and pathogenesis.

Ocular hypertension in Axenfeld-Rieger Syndrome.

Surgical outcomes of Glaucoma associated with Axenfeld-Rieger syndrome.

The diagnosis and phacoemulsification in combination with intraocular lens implantation for an Axenfeld-Rieger syndrome patient with small cornea: a case report.

Improvement of Open Bite and Stomatognathic Function in an Axenfeld- Rieger Syndrome Patient by Orthodontic Sectional Arch Mechanics: Clinical Considerations and the Risk of Orthodontic Tooth Movement.

Progressive High Hypermetropic Shift as a Refractive Surprise Following Glaucoma Filtration Surgery in a Phakic Child With Early-Onset Childhood Glaucoma Associated With Axenfeld-Rieger Anomaly.

Showing 1-11 of 11

Last Updated : 05/19/2022