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.
Original language | English (US) |
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Pages (from-to) | 1369-1371 |
Number of pages | 3 |
Journal | Journal of Clinical Sleep Medicine |
Volume | 15 |
Issue number | 9 |
DOIs | |
State | Published - Sep 15 2019 |
Externally published | Yes |
ASJC Scopus subject areas
- Clinical Neurology
- Neurology
- Pulmonary and Respiratory Medicine