There
are at least two types of prosopagnosia.
One
type is congenital or developmental
prosopagnosia where
there appears to be no brain damage. At this point it is a lifelong
facial-recognition deficit that typically manifests early in childhood. It has
a prevalence rate of 2.5 percent. Studies have shown this type to be completely
compatible with compatible with autosomal dominant inheritance.
There is also an acquired form that exhibits after the brain
has sustained some type of damage or injury, the type that Dr. Sacks addressed
in his book. Interestingly, instances have been reported
where acquired prosopagnosia spontaneously
resolved on its own. More tomorrow
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