Perry Disease: Concept of a New Disease and Clinical Diagnostic Criteria
Perry disease is a hereditary neurodegenerative disease with autosomal dominant inheritance. It is characterized by parkinsonism, psychiatric symptoms, unexpected weight loss, central hypoventilation, and transactive-response DNA-binding protein of 43kD (TDP-43) aggregation in the brain. In 2009, Pe...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
Korean Movement Disorders Society
2021-01-01
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| Series: | Journal of Movement Disorders |
| Subjects: | |
| Online Access: | http://www.e-jmd.org/upload/jmd-20060.pdf |