Four detailed cases of delusions of misidentification (DM) are presented: two cases of misidentification of the reflected self, one of reverse intermetamorphosis, and one of reduplicative paramnesia. The cases are discussed in the context of three levels of interpretation: neurological, cognitive and phenomenological. The findings are compared to previous work with DM patients, particularly the work of Ellis and Young (1990;Young, 1998) who found that loss of the normal affective response to familiar faces was a contributing factor in the Capgras delusion. The four cases presented suggest that this particular deficit is not a critical factor in the development of other forms of DM.Delusions of misidentification (DM) include a variety of fascinating disorders in which there is a mistaken belief in the identity of oneself, other people, places or objects. They include: Capgras syndrome-the belief that other people, often close relatives, have been replaced by doubles or impostors; Fregoli syndrome-the belief that strangers are in fact known people in disguise; intermetamorphosis-the belief that someone has changed physically and psychologically into another person; reverse intermetamorphosis-the belief that there has been a physical and psychological change of oneself into another person; and reduplicative paramnesia-the belief that there are doubles of known people or places. This last delusion (reduplicative paramnesia) differs from Capgras delusion in that while reduplication is believed to have occurred, there is no sense of replacement. Thus, the impostor claim is not made in cases of reduplicative paramnesia. Patients with DM traverse the boundaries of psychiatry, neurology and neuropsychology and have been studied from the perspective of all three disciplines. 1 We are very grateful to TH, FE, DB, RZ and their families for their participation in this research. We would also like to thank Matthew Large for insightful discussion about the cases and referral of patient RZ, Virginia Arpadi for referring patient TH, David Sharpe for referring patient FE, and Robyn Langdon and Karalyn Patterson for helpful comments on an earlier draft of this paper.