Perry syndrome is a rare, adult-onset, autosomal dominant, progressive neurodegenerative disorder that is characterized by parkinsonism, weight loss, psychiatric symptoms, and central hypoventilation. We report the case of a 51-year-old man, whose condition was genetically identified as Perry syndrome. Here we focus the polysomnographic (PSG) findings and discuss the correlations between PSG and neuropathological findings.
CITATION STYLE
Ji, K. H., Kang, M. R., Chung, E. J., & Kim, S. J. (2018). Sleep and respiration of Perry syndrome: Polysomnographic and pathological correlations. Sleep Medicine Research, 9(2), 115–117. https://doi.org/10.17241/smr.2018.00213
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