Srivastava et al. [6] also reported in 2021 a 7-year-old male patient with the WASF1:c.1516 C > T mutation who was intellectually disabled; seizures; axial hypotonia; speechless; head banging, hitting people; long face, simple ears; strabismus, exotropia (Table 1). Here, WASF1 is linked to Exotropia.