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Updated: Sep 29, 2026

Quantification of Orofacial Phenotypes in Xenopus
Published on: November 6, 2014
Newborn with anophthalmia and features of Fryns syndrome
Diane M Pierson1, Antonio Subtil, Eugenio Taboada
1Department of Pathology, Truman Medical Center, Kansas City, MO, USA.
Abstract:
We report a newborn female with craniofacial malformations, bilateral anophthalmia, large abnormally shaped ears, short neck, small distal phalanges and nails, left diaphragmatic hernia, hypoplastic optic nerves, severe pulmonary hypoplasia, and an accessory spleen, and describe the autopsy findings. The infant expired at 18 h of life. The features were most consistent with Fryns syndrome although other conditions were considered including Matthew Wood syndrome. Anophthalmia, to our knowledge, has not been reported previously in Fryns syndrome; however, eye findings are common, particularly microphthalmia and cloudy cornea.

