Figure 2
From: A De Novo FOXP1 Truncating Mutation in a Patient Originally Diagnosed as C Syndrome
Main features of the patient. (A–B) Neonatal CT scan. Trigonocephaly is clearly appreciated. For a control CT scan, see Khanna et al.32 (C–E) Facial dysmorphisms at 2 and 23 years of age. Hypertelorism, convergent strabismus, down slanted palpebral fissures, epicanthus, prominent nasal root and ante-verted nostrils and (F) arched palate and hypertrophy of the alveolar processes are appreciated. (G–H) Foot phenotype with metatarsal flat-footedness and clinodactyly. All images are shared by the family with explicit permission to publish.
