Submicroscopic 11p13 deletion including the elongator acetyltransferase complex subunit 4 gene in a girl with language failure, intellectual disability and congenital malformations: A case report

Figure 1 Patient at 1-year-old. A: Microcephaly, upward-slanting palpebral fissures, depressed nasal bridge, bulbous nose, bilateral cleft lip, and palate are showed; B: The brain magnetic resonance scan (at five months) shows cortical atrophy, simplified gyral cortical patterns (orange arrow) and band heterotopia (arrow ahead).