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It is well established that selective cognitive impairments may be present in amyotrophic lateral sclerosis (ALS) patients who do not display a full blown frontotemporal dementia (FTD) syndrome.1 ,2 Over the last 20 years there has been a surge of publications demonstrating predominantly executive dysfunction and most recently social cognition deficits in these patients.3–5 This may be taken as evidence of potentially subclinical levels of FTD in this group, enhancing the link between the two disorders with the demonstration of a spectrum of cognitive dysfunction from ALS patients who only display motor involvement (ALS-motor) to those with dementia (ALS-FTD).
The Taylor et al6 study makes a significant contribution to this field by highlighting the presence of language deficits in ALS patients without dementia, which although occasionally demonstrated for example,1 ,7 ,8 and certainly long suspected, is an area which has been relatively neglected. Previous investigations have often been …
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