A familial factor in the development of colour agnosia.

摘要: An important aspect of research into the link between genes and behaviour concerns identification familial determination. There is evidence for factors in selective deficits, such as developmental dyslexia prosopagnosia. Colour agnosia a neuropsychological condition which colour perception intact, while naming disrupted. We recently demonstrated that this deficit can occur deficit. Here, we show there factor development by reporting processing abilities mother daughters man with agnosia.