Fig. 1From: A de novo triplication on 2q22.3 including the entire ZEB2 gene associated with global developmental delay, multiple congenital anomalies and behavioral abnormalitiesThe proband at 2 years 2 months of age. Note scaphocephaly and flat facial profile, auricle dysplasia, low-set and asymmetrical ears, small eyes, flat nose bridge, shallow philtrum, small and open mouth, teeth dysplasia, micrognathia, sparse eyebrows and hair, short hands and broad fingersBack to article page