Behavior and sleep disturbance in Smith-Magenis syndrome.
Journal
Current opinion in psychiatry
ISSN: 1473-6578
Titre abrégé: Curr Opin Psychiatry
Pays: United States
ID NLM: 8809880
Informations de publication
Date de publication:
03 2019
03 2019
Historique:
pubmed:
18
12
2018
medline:
7
3
2020
entrez:
18
12
2018
Statut:
ppublish
Résumé
To provide an update of the most recent studies on Smith-Magenis syndrome (SMS) with a focus on the unique pattern of behavioral and sleep disturbances associated with the condition. The recent literature on SMS has focused on the characteristic severe behavioral and sleep disturbances. A better understanding of the underlying pathophysiological mechanisms and common clinical course has helped further characterize SMS, while much is left to be discovered in regard to effective treatment/management. SMS is a difficult to manage genetic condition defined by pervasive and progressive behavioral and sleep disturbances with a unique pattern that can often be easily discerned from other neurodevelopmental disorders. Common behavioral features include maladaptive/self-injurious, aggressive, stereotypic, and the newly appreciated food seeking behaviors associated with SMS. In addition, there is a sleep disturbance defined by an altered circadian rhythm with frequent nighttime waking and daytime sleepiness, causing patients and families significant distress. Small studies have suggested some treatment/management approaches to the behavioral and sleep disturbances, however, much remains to be discovered.
Identifiants
pubmed: 30557269
doi: 10.1097/YCO.0000000000000474
pmc: PMC6362978
mid: NIHMS1518768
doi:
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
73-78Subventions
Organisme : NIGMS NIH HHS
ID : T32 GM007526
Pays : United States
Références
Appl Clin Genet. 2017 Nov 03;10:85-94
pubmed: 29138588
Am J Ment Retard. 2001 Jan;106(1):52-8
pubmed: 11246713
J Autism Dev Disord. 2016 Jun;46(6):2148-2159
pubmed: 26983920
Invest Ophthalmol Vis Sci. 2018 Jan 1;59(1):362-369
pubmed: 29346496
J Assoc Genet Technol. 2005;31(4):163-7
pubmed: 16354942
J Autism Dev Disord. 2017 Aug;47(8):2602-2609
pubmed: 28500573
Am J Hum Genet. 1997 May;60(5):1184-93
pubmed: 9150166
Proc Natl Acad Sci U S A. 2018 Oct 16;115(42):10744-10749
pubmed: 30275311
CNS Neurosci Ther. 2016 Nov;22(11):928-935
pubmed: 27743421
Am J Med Genet A. 2011 Aug;155A(8):2024-7
pubmed: 21739587
Neuron. 2016 Oct 19;92(2):392-406
pubmed: 27693255
Pediatr Neurol. 2009 Oct;41(4):250-8
pubmed: 19748044
Diabetes. 2006 Dec;55(12):3366-71
pubmed: 17130481
Tijdschr Psychiatr. 2010;52(10):719-23
pubmed: 20931486
Am J Hum Genet. 2012 Jun 8;90(6):941-9
pubmed: 22578325
J Intellect Disabil Res. 1998 Oct;42 ( Pt 5):331-40
pubmed: 9828063
J Pediatr. 2006 Sep;149(3):409-11
pubmed: 16939758
Pediatr Neurol. 2006 May;34(5):337-50
pubmed: 16647992
J Med Genet. 2001 Sep;38(9):586-90
pubmed: 11546826
J Intellect Disabil Res. 2011 Feb;55(2):138-51
pubmed: 21199049
Clin Genet. 2007 Jun;71(6):540-50
pubmed: 17539903
Mol Cell Endocrinol. 2006 Jun 27;252(1-2):88-91
pubmed: 16723183
J Clin Endocrinol Metab. 2012 Feb;97(2):E312-8
pubmed: 22162479
BMJ Case Rep. 2016 Aug 05;2016:
pubmed: 27495174
Am J Med Genet C Semin Med Genet. 2010 Nov 15;154C(4):463-8
pubmed: 20981776
J Neurodev Disord. 2018 Jan 10;10(1):2
pubmed: 29329513
Orphanet J Rare Dis. 2015 Sep 04;10:111
pubmed: 26336863
Res Dev Disabil. 2015 Dec;47:27-38
pubmed: 26323055
Curr Opin Neurol. 2007 Apr;20(2):125-34
pubmed: 17351481
Res Dev Disabil. 2013 Dec;34(12):4355-65
pubmed: 24120292
Neurosci Biobehav Rev. 2018 Jan;84:483-491
pubmed: 28694012
J Speech Lang Hear Res. 2017 Apr 14;60(4):1076-1087
pubmed: 28384694
Hum Mol Genet. 2010 Oct 15;19(20):4026-42
pubmed: 20663924
Genet Med. 2006 Jul;8(7):417-27
pubmed: 16845274
Phys Occup Ther Pediatr. 2012 Feb;32(1):48-65
pubmed: 21599572
J Pediatr Genet. 2017 Sep;6(3):155-164
pubmed: 28794907
J Neurodev Disord. 2018 Mar 1;10(1):9
pubmed: 29490614
Am J Med Genet A. 2017 Jan;173(1):231-238
pubmed: 27683195
Am J Med Genet. 1998 Apr 28;77(1):23-7
pubmed: 9557889