Abstract
Idiopathic rapid eye movement sleep behavior disorder is characterized by vocalizations and complex motor behaviors during sleep. We report a case of a 44-year-oldmale with a 20-year history of dream enactment behavior that was incidentally captured on a polysomnogramduring an evaluation for obstructive sleep apnea. Genetic testing found the patient had a homozygous deletion for one of the five tandemrepeats in exon 18 of the PER3 gene. This case highlights a potential genetic basis for idiopathic rapid eye movement sleep behavior disorder.
Cite
CITATION STYLE
Brock, M. S., Shirley, S., Rohena, L., Moore, B. A., & Mysliwiec, V. (2019). Unexpected finding of idiopathic REM sleep behavior disorder in a young healthy male with snoring: A case report. Journal of Clinical Sleep Medicine, 15(9), 1369–1371. https://doi.org/10.5664/jcsm.7938
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.