Cited by 31Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental DisordersAttention Deficit Hyperactivity Disorder

Pharmacological treatment of disruptive behavior in Smith–Magenis syndrome

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Laje, Gonzalo, Bernert, Rebecca, Morse, Rebecca, Pao, Maryland, Smith, Ann C.M.·2010·American Journal of Medical Genetics Part C: Seminars in Medical Genetics

Abstract

Smith–Magenis syndrome (SMS) is a complex genetic syndrome caused by an interstitial deletion of chromosome 17p11.2. Children and adults with SMS appear to have unique neurobehavioral problems that include: sleep disturbance, self‐injurious and maladaptive behaviors, stereotypies, and sensory integration disorders. We gathered retrospective psychotropic use information from parents or other caregivers of 62 individuals with SMS who were asked about use of psychotropic medication from a list of commonly used psychiatric medications. For those drugs identified, respondents were asked to rate the experience with the particular medication using a likert‐type scale. Drugs were grouped into seven main categories: (1) stimulants; (2) antidepressants; (3) antipsychotics; (4) sleep aides; (5) mood stabilizers; (6) alpha 2 agonists; and (7) benzodiazepines. Relative frequencies, means and standard deviations pertaining to age and medication effect were derived for each medication category. Six of the seven medication categories examined showed no meaningful deviations from the “no change” score. The benzodiazepine group showed a mild detrimental effect. There were no gender differences in efficacy. Use of psychotropic medication started early in life (mean age 5 years), particularly with sleep aides. Although no medication category was identified as efficacious in SMS, all the categories reported herein may be considered as an option for brief symptomatic relief. Published 2010 Wiley‐Liss, Inc.

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  • Other monogenic syndromes like Kleefstra, KBG, WitKoS, Angelman, Coffin-Sirris, Rubinstein-Taybi, Phelan-McDermid, Smith-Magenis Syndrome and Kabuki syndrome also have a clear prefrontal component in their behavioral and cognitive phenotype.

    “Other monogenic syndromes like Kleefstra, KBG, WitKoS, Angelman, Coffin-Sirris, Rubinstein-Taybi, Phelan-McDermid, Smith–Magenis Syndrome and Kabuki syndrome also have a clear prefrontal component in their behavioral and cognitive phenotype [272–280].”

    From Development of prefrontal cortex (2022) · cites this paper as [278]

    The Introduction describes Smith–Magenis syndrome as a genetic syndrome with intellectual disability and distinctive neurobehavioral problems; the Discussion also mentions inattention and impulsivity. But neither passage identifies a prefrontal component of its behavioral or cognitive phenotype. This source supports the Smith–Magenis phenotype portion of the multi-syndrome sentence, not its prefrontal characterization. (LLM, conf=0.84)

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References 18 · Cited by 31

Research works printed but not linked: 2

  1. Duncan W Gropman A Morse R Krasnewich D Smith ACM Good Babies Sleeping Poorly: Insufficient Sleep in Infants with Smith-Magenis Syndrome (SMS) Am J Hum Genet (suppl) 2003 73 5 A896
  2. Smith AC Dykens E Greenberg F Sleep disturbance in Smith-Magenis syndrome (del 17 p11.2) Am J Med Genet 1998b 81 2 186 91 9613860

Authors
Laje, G., Bernert, R., Morse, R., Pao, M., & Smith, A. C. M.
Affiliations
  • National Institutes of Health (US)
  • Florida State University (US)
  • George Mason University (US)
Corresponding author
Laje, Gonzalo
Venue
American Journal of Medical Genetics Part C: Seminars in Medical Genetics
Publisher
Wiley
Published
2010-10-27
Volume
154C
Issue
4
Pages
463-468
ISSN
  • 1552-4868 (ISSN-L)
  • 1552-4876
OpenAlex
W2171192059
Cited by
31
References
18
Citations by year
2026: 1 · 2025: 1 · 2024: 2 · 2022: 3 · 2021: 3 · 2020: 4 · 2019: 1 · 2018: 1 · 2017: 1 · 2016: 2 · 2015: 3 · 2014: 1 · 2013: 4
FWCI
1.44
Type
journal article
Language
en
Open access
Locations
  • American Journal of Medical Genetics Part C Seminars in Medical Genetics (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • National Institutes of Health (Z99 MH999999)
  • National Institute of Mental Health
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genomic variations and chromosomal abnormalities
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
  • Health Sciences › Medicine › Psychiatry and Mental health › Attention Deficit Hyperactivity Disorder
Keywords
Smith-Magenis syndrome, disruptive behavior, psychotropic drugs, pharmacotherapy, chromosome 17p11.2 deletion, sleep disorders, self-harm, stimulants, antidepressants, antipsychotic drugs, sleep aids, benzodiazepines, alpha-2 adrenergic agonists, mood stabilizers, drug efficacy
MeSH terms
Adult, Age Factors, Analysis of Variance, Child, Female, Humans, Male, Psychotropic Drugs, Surveys and Questionnaires, Retrospective Studies, Treatment Outcome, Attention Deficit and Disruptive Behavior Disorders, Smith-Magenis Syndrome

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