Table 1.
Neurodevelopmental disorders showing global motion sensitivity impaired relative to global form sensitivity
Disorder group | Origin | Reference |
---|---|---|
young Williams Syndrome children | genetic | Atkinson et al (1997, 2003) |
adult Williams Syndrome | genetic | Atkinson et al (2006) |
autism | possibly genetic | Spencer et at (2002); Simmons et al (2009) |
hemiplegic children | acquired | Gunn et al (2002) |
developmental dyslexia | ? | Hansen et al (2001) |
fragile X | genetic | Kogan et al (2004) |
very preterm born’ | acquired | Atkinson et al, 2007; Taylor et al (2009) |
congenital cataract | acquired? | compare Ellemberg et al, (2002) with Lewis et al (2002) |
strabismic amblyopia | acquired? | Simmers et al (2005) ; Ho et al (2005) |