1. Jactatio capitis nocturna with persistence in adulthood. Case report.
- Author
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Alves RS, Alóe F, Silva AB, and Tavares SM
- Subjects
- Adult, Antidepressive Agents, Tricyclic therapeutic use, Humans, Imipramine therapeutic use, Male, Periodicity, Polysomnography, Sleep Wake Disorders drug therapy, Stereotypic Movement Disorder drug therapy, Sleep Wake Disorders diagnosis, Sleep, REM, Stereotypic Movement Disorder diagnosis
- Abstract
Rhythmic movement disorder, also known as jactatio capitis nocturna, is an infancy and childhood sleep-related disorder characterized by repetitive movements occurring immediately prior to sleep onset and sustained into light sleep. We report a 19-year-old man with a history of headbanging and repetitive bodyrocking since infancy, occurring on a daily basis at sleep onset. He was born a premature baby but psychomotor milestones were unremarkable. Physical and neurological diagnostic workups were unremarkable. A hospital-based sleep study showed: total sleep time: 178 min; sleep efficiency index 35.8; sleep latency 65 min; REM latency 189 min. There were no respiratory events and head movements occurred at 4/min during wakefulness, stages 1 and 2 NREM sleep. No tonic or phasic electromyographic abnormalities were recorded during REM sleep. A clinical diagnosis of rhythmic movement disorder was performed on the basis of the clinical and sleep studies data. Clonazepam (0.5 mg/day) and midazolam (15 mg/day) yielded no clinical improvement. Imipramine (10 mg/day) produced good clinical outcome. In summary, we report a RMD case with atypical clinical and therapeutical features.
- Published
- 1998
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