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Prosopagnosia



Prosopagnosia
Classification & external resources
MeSH D020238

Prosopagnosia (sometimes known as face blindness) is a disorder of face perception where the ability to recognize faces is impaired, while the ability to recognize other objects may be relatively intact. The term usually refers to a condition following acute brain damage, but recent evidence suggests that a congenital form of the disorder may exist. The specific brain area usually associated with prosopagnosia is the fusiform gyrus.[1]

Few successful therapies have so far been developed for affected people, although individuals often learn to use 'piecemeal' or 'feature by feature' recognition strategies. This may involve secondary clues such as clothing, hair color, body shape, and voice. Because the face seems to function as an important identifying feature in memory, it can also be difficult for people with this condition to keep track of information about people, and socialize normally with others.

Some also use the term prosophenosia, which refers to the inability to recognize faces following extensive damage of both occipital and temporal lobes.[2][3]

Contents

Overview

Selective inabilities to recognize faces were reported throughout the 19th century, and included case studies by Hughlings Jackson and Charcot. However, it was not named until the term prosopagnosia was first used in 1947 by Joachim Bodamer, a German neurologist. He described three cases, including a 24-year old man who suffered a bullet wound to the head and lost his ability to recognise his friends, family, and even his own face. However, he was able to recognize and identify them through other sensory modalities such as auditory, tactile, and even other visual stimuli patterns (such as gait and other physical mannerisms). Bodamer gave his paper the title Die Prosop-Agnosie, derived from classical Greek πρόσωπον (prosopon) meaning "face" and αγνωσία (agnosia) meaning "non-knowledge".

The study of prosopagnosia has been crucial in the development of theories of face perception. Because prosopagnosia is not a unitary disorder (i.e., different people may show different types and levels of impairment) it has been argued that face perception involves a number of stages, each of which can be separately damaged.[4] This is reflected not just in the amount of impairment displayed but also in the qualitative differences in impairment that a person with prosopagnosia may present with.

This sort of evidence has been crucial in supporting the theory that there may be a specific face perception system in the brain. This is counter-intuitive to many people as we do not experience faces as 'special' or perceived in a different way from the rest of the world.

There is some debate about the specificity of both face perception and prosopagnosia and some people have argued that it is just a subtype of visual agnosia. Whilst prosopagnosia is often accompanied by problems with recognising visual objects, cases have been reported where perception for faces seems to be selectively impaired.[5]

It has also been argued that prosopagnosia may be a general impairment in understanding how individual perceptual components make up the structure or gestalt of an object. Psychologist Martha Farah has been particularly associated with this view.

Until early in the 21st century, prosopagnosia was thought to be quite rare and solely associated with brain injury or neurological illness affecting specific areas of the brain. However, some evidence suggests that there may be a form of congenital prosopagnosia in which people are born with a selective impairment in recognising and perceiving faces. The cases that have been reported suggest that this form of the disorder may be highly variable and some newer research suggests that it may be heritable and much more common than previously thought (about 2% of the population may be affected).[6][7] It has been suggested that very mild cases of face blindness are much more common, perhaps affecting 10% of the population, although there have not been any studies confirming this.[1] The ability to keep track of the identity of characters in movies is a common complaint(see [[1]]).

Subtypes of prosopagnosia

Apperceptive prosopagnosia

Apperceptive prosopagnosia is thought to be a disorder of some of the earliest processes in the face perception system. People with this disorder cannot make any sense of faces and are unable to make same-different judgements when they are presented with pictures of different faces. They may also be unable to work out attributes such as age or gender from a face. However, they may be able to recognise people based on non-face clues such as their clothing, hairstyle or voice.

Associative prosopagnosia

Associative prosopagnosia is thought to be an impairment to the links between early face perception processes and the semantic information we hold about people in our memories. People with this form of the disorder may be able to say whether photos of people's faces are the same or different and derive the age and gender from a face (suggesting they can make sense of some face information) but may not be able to subsequently identify the person or provide any information about them such as their name, occupation or when they were last encountered. They may be able to recognise and produce such information based on non-face information such as voice, hair, or even particularly distinctive facial features (such as a distinctive moustache) that does not require the structure of the face to be understood. Typically such people do not report that 'faces make no sense' but simply that they do not look distinctive in any way.

Developmental prosopagnosia

Developmental prosopagnosia is thought to be a form of 'congenital prosopagnosia', and that some people are born with a selective impairment in recognising and perceiving faces. The cases that have been reported suggest that this form of the disorder may be highly variable and there is some suggestion that it may be hereditary.

  • Developmental disorders such as autism and Williams syndrome are known to also involve differences in face perception, but the mechanism by which these effects take place is largely unknown.

Unconscious face recognition

One particularly interesting feature of prosopagnosia is that it suggests both a conscious and unconscious aspect to face recognition. Experiments have shown that when presented with a mixture of familiar and unfamiliar faces, people with prosopagnosia may be unable to successfully identify the people in the pictures, or even make a simple familiarity judgement ("this person seems familiar / unfamiliar"). However, when a measure of emotional response is taken (typically a measure of skin conductance) there tends to be an emotional response to familiar people even though no conscious recognition takes place[8]

This suggests emotion plays a significant role in face recognition, perhaps unsurprising when basic survival (particularly security) relies on identifying the people around you.

It is thought that Capgras delusion may be the reverse of prosopagnosia. In this condition people report conscious recognition of people from faces, but show no emotional response, perhaps leading to the delusional belief that their relative or spouse has been replaced by an impostor.

See also

At Wikiversity, you can learn about:
prosopagnosia

References

  1. ^ a b Face blindness not just skin deep - CNN.com
  2. ^ Paulev, Poul-Erik (1999 - 2000). Textbook in Medical Physiology And Pathophysiology Essentials and clinical problems. Copenhagen Medical Publishers. ISBN 87-984078-0-5.  Chapter 4. Brain Function, Locomotion And Disorders
  3. ^ Weis. "Nervous System Pathways". Biol 2401 A & P Lecture Notes.
  4. ^ Dissociable deficits after brain injury by Newcombe, F., de Haan, E.H.F., Small, M. & Hay, D.C. in Young, Andrew W. (1998). Face and Mind. Oxford: Oxford University Press. ISBN 0-19-852420-X. 
  5. ^ (1977) "Prosopagnosia: A clinical, psychological and anatomical study of three patients". Journal of Neurology, Neurosurgery and Psychiatry (40): 395-403.
  6. ^ Kennerknecht I, Grueter T, Welling B, Wentzek S, Horst J, Edwards S, Grueter M. "First report of prevalence of non-syndromic hereditary prosopagnosia (HPA)." Am J Med Genet A. 2006 Aug 1;140(15):1617-22. PMID 16817175.
  7. ^ (26 March 2005) "New Scientist".
  8. ^ Bauer, R.M. (1984) Autonomic recognition of names and faces in prosopagnosia: A neuropsychological application of the guilty knowledge test. Neuropsychologia, 22, 457-469

Further reading

  • Bruce, V. and Young, A. (2000) In the Eye of the Beholder: The Science of Face Perception. Oxford: Oxford University Press. ISBN 0-19-852439-0
  • Cante, Richard C. (March 2008). Gay Men and the Forms of Contemporary US Culture. London: Ashgate Publishing. ISBN: 0 7546 7230 1. Chapter 7: The Gay Visage (and Related Forms of Thought). 
  • Farah, M.J. (1990) Visual agnosia: Disorders of object recognition and what they tell us about normal vision. MIT: MIT Press. ISBN 0-262-06238-0
  • (December 2 2004) "About face". Economist.
  • (October 19 2006) "Your mother's smile". Economist. Evidence mounts that making, and perhaps recognising, expressions is inherited
  • Abedin, Shahreen (February 5 2007). "Face blindness not just skin deep". CNN.com.
 
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Prosopagnosia". A list of authors is available in Wikipedia.
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