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 Disorder 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 |