Familial Transmission of Developmental Prosopagnosia: New Case Reports from an Extended Family and Identical Twins.
face perception
face recognition
genetics
heritability
prosopagnosia
Journal
Brain sciences
ISSN: 2076-3425
Titre abrégé: Brain Sci
Pays: Switzerland
ID NLM: 101598646
Informations de publication
Date de publication:
04 Jan 2024
04 Jan 2024
Historique:
received:
06
11
2023
revised:
13
12
2023
accepted:
31
12
2023
medline:
22
1
2024
pubmed:
22
1
2024
entrez:
22
1
2024
Statut:
epublish
Résumé
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.
Identifiants
pubmed: 38248264
pii: brainsci14010049
doi: 10.3390/brainsci14010049
pii:
doi:
Types de publication
Journal Article
Langues
eng
Subventions
Organisme : Leverhulme Trust
ID : RF-2020-105