Fig. 1
From: Molecular and clinical characterization of new patient with 1,08 Mb deletion in 10p15.3 region
a Patient on the first day of life: round face, long palpebral fissures, epicanthal folds, wide nasal root and wide nasal bridge. b Patient at the age 8 months: round face, upstanding palpebral fissures, low set nasal root, short columella, narrow upper lip, long and protruding ears. c Patient at the age 2 years: frontal bossing, ocular hypertelorism, long upstanding palpebral fissures, long lashes, low set nasal root, wide nasal bridge, narrow upper lip, short chin