Fig. 2From: Cardio-facio-cutaneous syndrome and gastrointestinal defects: report on a newborn with 19p13.3 deletion including the MAP 2 K2 genea. Patient’s front view: coarse face and asymmetry due to left hypoplasia, high and prominent forehead, hypoplastic supraorbital ridges, sparse and friable hair, eyebrows and eyelashes, wide and depressed nasal bridge, bulbous tip, anteverted nares, long philtrum; b. Lateral view: bilateral small, dysplastic, crumbled and posteriorly rotated ears with thickened helices and right preauricular tagBack to article page