Fig. 1From: Compound phenotype in a girl with r(22), concomitant microdeletion 22q13.32-q13.33 and mosaic monosomy 22The patient at 4 years of age (note plagiocephaly, high anterior hairline, broad forehead, epicanthus, widely spaced eyes, upslanted palpebral fissure, upper eyelid fullness, straight eyebrows, prominent ears, wide and depressed nasal bridge, bulbous nose, smooth and short philtrum, and thin vermillion of the upper lip)Back to article page