Figure 2From: A boy with homozygous microdeletion of NEUROG1 presents with a congenital cranial dysinnervation disorder [Moebius syndrome variant]The proband at age 3 ½ years. Note (A) hypotonic appearance, balance disorder and torticollis, (B, C) scaphocephaly, high arched eyebrows, elongated palpebral fissures and low-set posteriorly rotated ears, and (D) orthopedic aids for correction of faulty foot posture.Back to article page