“…This would exclude mere IFR difficulties without complete impairment of the function, which are found in a large fraction of the population with right posterior brain damage (Benton & Van Allen, ; Valentine, Powell, Davidoff, Letson, & Greenwood, ; Young, Newcombe, de Haan, Small, & Hay, ), but also IFR impairments occurring during development, in a system that has not reached a high level of expertise at IFR (i.e., no ‘childhood prosopagnosia’, Young & Ellis, ). In the same vein, IFR difficulties in patients with a long history of temporal epilepsy (e.g., Drane et al ., ), neurodegenerative disorders such as Alzheimer's disease (e.g., Lavallée et al ., ), the right temporal pole variant of frontotemporal dementia (Rtv‐FTLD (e.g., Busigny, Robaye, Dricot, & Rossion, ; Joubert et al ., ) or yet diffuse low‐grade gliomas (e.g., Corrivetti, Herbet, Moritz‐Gasser, & Duffau, ) should not be labelled (i.e., put in the same basket) as cases of prosopagnosia.…”