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Mirtazapine for sleep disturbances in Angelman syndrome: a retrospective chart review of 8 pediatric cases
Author(s) -
Emily Hanzlik,
Sarah A. Klinger,
Robert P. Carson,
Jessica Duis
Publication year - 2020
Publication title -
journal of clinical sleep medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 92
eISSN - 1550-9397
pISSN - 1550-9389
DOI - 10.5664/jcsm.8284
Subject(s) - mirtazapine , medicine , angelman syndrome , sleep (system call) , polysomnography , psychiatry , pediatrics , audiology , electroencephalography , antidepressant , anxiety , biochemistry , chemistry , gene , computer science , operating system
Angelman syndrome (AS) is a rare neurodevelopmental disorder that is characterized by developmental delay, intellectual disability, seizures, a characteristic happy personality, gait ataxia, tremulousness of the limbs, microcephaly, and anxiety. Severe sleep disturbances with the diminished need for sleep and abnormal sleep-wake cycles are seen in up to 90% of patients with AS. AS is caused by absent maternal expression of the gene UBE3A located in the 15q11.2-q13 locus. We hypothesized that selective antagonism of 5-HT₂ and 5-HT₃ serotonin receptors with mirtazapine would benefit sleep disturbances in patients with AS.

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