Fig. 3From: Whole-exome sequencing identifies homozygous mutation in TTI2 in a child with primary microcephaly: a case reportPatient’s phenotypic features. a-d Samples pictures of the described patient 1 month before his fourth birthday. We can denote the strabismus (a), a deep set of eyes (b), a high palate (c) and the forehead with prominent metopic ridge (d)Back to article page