Mapping the imageless mind: Towards a taxonomy of aphantasia
BartolomeoNovember 2025
Abstract
Although cases of absent mental imagery have been reported for more than a century (Galton, 1880), systematic investigation was reignited by Zeman et al. (2015), who introduced the term congenital aphantasia to describe the lifelong inability to form mental images. Their work triggered a surge of studies producing diverse and sometimes contradictory conclusions. The lack of a taxonomy may contribute to this confusion by conflating different phenomena under a single label. While Zeman and colleagues described this phenomenon in otherwise healthy individuals, similar phenomena have also been observed in clinical populations. Since Charcot’s seminal description of Monsieur X (Charcot and Bernard, 1883) (see Bartolomeo, 2008 for an English translation), neurologists have documented acquired cases of imagery loss (reviews in Bartolomeo, 2002, 2008; Bartolomeo et al., 2020; Goldenberg, 1993; Spagna, 2022). Yet, in some cases, including Monsieur X, the abrupt disappearance of imagery has been argued to reflect psychogenic rather than organic origins (Zago et al., 2011). These observations indicate that aphantasia is a heterogeneous phenomenon, and suggest the existence of at least three distinct forms: neurological, psychogenic, and congenital aphantasia.
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What They Found
- Neurological aphantasia can follow brain damage, such as extensive lesions of the temporal lobe. Left temporal damage typically removes imagery in general, or only for objects, colors or letters. The author suggests a left fusiform region, the Fusiform Imagery Node, may be a key node of the imagery network; a preprint on 12 patients found it damaged or disconnected in every case. Another acquired form, imaginal neglect, typically after right-hemisphere damage, leaves people unable to describe the left side of their mental images.
- Psychogenic aphantasia accompanies psychiatric symptoms such as anxiety, depression and depersonalization (feeling detached from oneself). The author suggests it may partly reflect problems processing bodily signals (interoception) and calls it the least studied form. Mixed neurological and psychiatric cases may also exist; Charcot's 1883 patient, "Monsieur X," may be one.
- Congenital aphantasia is lifelong in otherwise healthy people and ranges from no imagery to faint impressions; the author cites prevalence estimates of 1 to 4%. People keep their visual knowledge but, he argues, cannot access it in a perception-like way. He cites an ultra-high-field brain imaging study (Liu and colleagues, 2025) in which the imagery node was active in aphantasia but more weakly coupled with prefrontal regions.
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Authors
Paolo Bartolomeo
11 papers in the library
Cite this paper
Bartolomeo, P. (2025). Mapping the imageless mind: towards a taxonomy of aphantasia. Neuropsychologia, 219, 109276. doi:/10.1016/j.neuropsychologia.2025.109276
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