Introduction
Prosopagnosia is a disease that reduces a
personís ability to recognize and identify familiar faces. The term is derived
from the Greek word for ìfaceî (prosopon) and ìnot knowingî (agnosia). It is
one of many forms of visual agnosia, and is caused by
lesions in the medial occipitotemporal region of the brain (Takamura
1996).
İİİİİİİ Patients with prosopagnosia know that a
face is a face, and know what different parts of the face are, but are unable
to name whom the familiar face belongs (Damasio
1982).
İİİİİİİ The symptoms of prosopagnosia were first
described by Wilbrand in 1892, but the term was coined by Joachim Bodamer in
1947 (Takamura 1996).İ Bodamerís patient
was a 24-year old man who suffered from a bullet-wound injury to the head.İ The man was of normal intelligence and
memory, but couldnít recognize the faces of himself, his friends, his family,
or even his dog (Szpir 1992).İ He could,
however, still identify people through other means such as listening to them,
touching them, or watching how they move.İ
İİİİİİİ The understanding of prosopagnosia and
the general process of face perception go hand in hand.İ Because prosopagnosia is not a unitary disorder it has been argued that face perception
involves a number of stages, each of which can be separately damaged. This is
shown in the wide range of impairments that a patient with prosopagnosia can
have ñ both qualitative and quantitative (Bruce 1986).
İİİİİİİ Originally, it was thought that
prosopagnosia was only associated with a brain injury acquired during
adulthood, but recent studies show it occurring in childhood development as well.İ Prosopagnosia is a very rare disease, which
means that case studies have been very important in the study of and theories
about this disease.
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