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. Author manuscript; available in PMC: 2013 Jan 29.
Published in final edited form as: Curr Opin Ophthalmol. 2011 Sep;22(5):314–324. doi: 10.1097/ICU.0b013e328349412b

Fig 1. Photographs of Patient with PITX2 regulatory region deletion and Axenfeld-Rieger syndrome.

Fig 1

*Previously Published*

Legend: A. Facial photograph showing maxillary hypoplasia, thin upper lip, and broad nasal bridge. B. Left eye corectopia. C. Right eye posterior embryotoxon. D. Dental anomalies, including maxillary hypodontia. E. Redundant periumbilical skin.

Source: Figure 5 from Volkmann BA, Zinkevich NS, Mustonen A, et al. Potential novel mechanism for Axenfeld-Rieger syndrome: deletion of a distant region containing regulatory elements of PITX2. Invest Ophthalmol Vis Sci 2011, 52(3):1450-1459.