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The first comprehensive case study of early-emerging prosopometamorphopsia.
Sydney Fortner1,2, Antônio Mello1, Daniel Stehr1
1Department of Psychological and Brain Sciences, Dartmouth College, Hanover, NH, USA 03755.
Prosopometamorphopsia (PMO) is a rare disorder causing lifelong facial distortions and misidentifications. This study details a unique case, offering insights into its early onset and neural basis.
Area of Science:
- Neuroscience
- Perceptual Psychology
- Clinical Neurology
Background:
- Prosopometamorphopsia (PMO) is a rare perceptual disorder.
- Facial distortions are a key characteristic of PMO.
- Early-onset cases of PMO are not well-documented.
Purpose of the Study:
- To conduct the first thorough study of an early-emerging case of Prosopometamorphopsia (PMO).
- To investigate the manifestations, co-occurring disorders, and neural correlates of lifelong PMO.
Main Methods:
- Case study of an individual with lifelong Prosopometamorphopsia (PMO).
- Behavioral assessments of facial distortions and identity recognition.
- Neuropsychological testing for face-processing abilities.
- Structural MRI and diffusion tensor imaging for neural correlates.
Main Results:
- The participant experienced dynamic, lifelong facial distortions and identity misrecognitions.
- Distortions were consistent across various viewing conditions.
- Face identity recognition deficits were observed, but accurate age and sex judgments were possible.
- Reduced face-selectivity in posterior areas and lower white matter integrity in the left inferior fronto-occipital fasciculus were found.
Conclusions:
- This case provides novel insights into early-emerging Prosopometamorphopsia (PMO).
- It highlights the co-occurrence of PMO with other face-processing deficits.
- It identifies potential underlying neural mechanisms, including white matter abnormalities.
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