Bate Sarah, Murray Ebony, Bennetts Rachel J
Department of Psychology, Bournemouth University, Poole BH12 5BB, UK.
Department of Psychological Sciences, School of Natural and Social Sciences, University of Gloucestershire, Cheltenham GL50 4AZ, UK.
Brain Sci. 2024 Jan 4;14(1):49. doi: 10.3390/brainsci14010049.
Existing evidence suggests that developmental prosopagnosia (DP) is a surprisingly prevalent condition, with some individuals describing lifelong difficulties with facial identity recognition. Together with case reports of multiple family members with the condition, this evidence suggests that DP is inherited in at least some instances. Here, we offer some novel case series that further support the heritability of the condition. First, we describe five adult siblings who presented to our lab with symptoms of DP. Second, for the first known time in the literature, we describe a pair of adult identical twins who contacted us in the belief that they both experience DP. The condition was confirmed in three of the five siblings (with minor symptoms observed in the remaining two) and in both twins. Supplementary assessments suggested that all individuals also experienced some degree of difficulty with facial identity perception, but that object recognition was preserved. These findings bolster the evidence supporting the heritability of DP and suggest that it can be a specific impairment in some cases.
现有证据表明,发展性面孔失认症(DP)是一种出人意料的普遍病症,一些患者称自己在面部识别方面存在终身困难。结合多个家庭成员患有该病症的病例报告,这些证据表明,至少在某些情况下,DP是可遗传的。在此,我们提供了一些新的病例系列,进一步支持了该病症的遗传性。首先,我们描述了五名成年兄弟姐妹,他们因DP症状前来我们实验室就诊。其次,在文献中首次有记载,我们描述了一对成年同卵双胞胎,他们联系我们,认为自己都患有DP。五名兄弟姐妹中有三名被确诊患有该病症(其余两名有轻微症状),双胞胎两人均被确诊。补充评估表明,所有个体在面部识别感知方面也都有一定程度的困难,但物体识别能力未受影响。这些发现进一步支持了DP具有遗传性的证据,并表明在某些情况下,它可能是一种特定的损伤。