Prosopagnosia (congenital vs. acquired) Flashcards
What is prosopagnosia?
A condition characterised by difficulty to recognise faces
What are the two main types of prosopagnosia?
Congenital and Acquired
What is another term for Congenital Prosopagnosia?
Developmental or Hereditary Prosopagnosia
How is Congenital Prosopagnosia defined?
Failure to develop face recognition ability without neurological illness or brain injury
What is the prevalence rate of Congenital Prosopagnosia according to Kennerknecht et al. (2006)?
2.5%
What are the symptoms of Congenital Prosopagnosia?
Irritation/uncertainty in recognizing faces, failure to recognize familiar faces, wrongly recognizing unfamiliar faces
What evidence suggests a genetic basis for Congenital Prosopagnosia?
All 14 participants who had CP had family members with CP
When does Congenital Prosopagnosia typically onset?
In childhood
What structural difference is associated with Congenital Prosopagnosia?
Differences in the Fusiform Face Area (FFA)
Is Congenital Prosopagnosia associative or apperceptive?
Associative
How is Acquired Prosopagnosia characterised?
A heterogeneous disorder with variability in symptoms and lesion sites
What are the two types of Acquired Prosopagnosia?
Apperceptive and Associative
Describe apperceptive and associative prosopagnosia.
Apperceptive - failure to perceive face structure. Associative - failure to link face with identity or semantic knowledge.
What brain areas are linked to deficits in face processing in Acquired Prosopagnosia?
Occipital Face Area (OFA) and Fusiform Face Area (FFA)
What is the primary treatment approach for Congenital Prosopagnosia?
Behavioural strategies