Ontology highlight
ABSTRACT: None
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-old male with a 20-year history of dream enactment behavior that was incidentally captured on a polysomnogram during an evaluation for obstructive sleep apnea. Genetic testing found the patient had a homozygous deletion for one of the five tandem repeats in exon 18 of the PER3 gene. This case highlights a potential genetic basis for idiopathic rapid eye movement sleep behavior disorder.Citation
Brock MS, Shirley S, Rohena L, Moore BA, Mysliwiec V. Unexpected finding of idiopathic REM sleep behavior disorder in a young healthy male with snoring: a case report. J Clin Sleep Med. 2019;15(9):1369-1371.
SUBMITTER: Brock MS
PROVIDER: S-EPMC6760398 | biostudies-literature | 2019 Sep
REPOSITORIES: biostudies-literature
Brock Matthew S MS Shirley Sean S Rohena Luis L Moore Brian A BA Mysliwiec Vincent V
Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine 20190901 9
<h4>None</h4>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-old male with a 20-year history of dream enactment behavior that was incidentally captured on a polysomnogram during an evaluation for obstructive sleep apnea. Genetic testing found the patient had a homozygous deletion for one of the five tandem repeats in exon 18 of the PER3 gene. This case highlights a potential genetic ba ...[more]