scholarly journals Psychometric Study of the Aberrant Behavior Checklist in Fragile X Syndrome and Implications for Targeted Treatment

2011 ◽  
Vol 42 (7) ◽  
pp. 1377-1392 ◽  
Author(s):  
Stephanie M. Sansone ◽  
Keith F. Widaman ◽  
Scott S. Hall ◽  
Allan L. Reiss ◽  
Amy Lightbody ◽  
...  
2013 ◽  
Vol 164 (1) ◽  
pp. 141-155 ◽  
Author(s):  
Anne Wheeler ◽  
Melissa Raspa ◽  
Carla Bann ◽  
Ellen Bishop ◽  
David Hessl ◽  
...  

PEDIATRICS ◽  
1995 ◽  
Vol 95 (5) ◽  
pp. 744-752 ◽  
Author(s):  
Thomas L. Baumgardner ◽  
Allan L. Reiss ◽  
Lisa S. Freund ◽  
Michael T. Abrams

Objective. A controlled clinical study was designed to identify the neurobehavioral profile that is specific to males with fragile X syndrome. Design. Thirty-one males with fragile X syndrome and 30 age and IQ-matched male controls were evaluated with instruments that assess multiple domains of adaptive functioning and problem behaviors. The Vineland Adaptive Behavior Scales and the Aberrant Behavior Checklist were selected for their dimensional scaling of behavioral ratings. Results. Parent and Teacher versions of the Aberrant Behavior Checklist demonstrated a profile of behaviors specific to males with fragile X syndrome characterized by significantly higher levels of hyperactivity, stereotypic movements, and unusual speech. The Vineland Adaptive Behavior Scales revealed no fragile X-specific profile of adaptive skills development. Conclusions. The distinct pattern of aberrant behaviors observed among males with fragile X emphasizes the importance of drawing subtype distinctions within the classification of individuals with mental retardation on the basis of underlying etiology. For clinical research, specifying the fragile X phenotype is a vital part in the effort to elucidate the neurodevelopmental pathways of normal behavior and psychopathology. Understanding the fragile X symptom pattern is essential for designing symptom-specific treatment interventions, as well as for research into the efficacy of interventions strategies.


2020 ◽  
Vol 30 (8) ◽  
pp. 512-521
Author(s):  
Michael G. Aman ◽  
Megan Norris ◽  
Aaron J. Kaat ◽  
Howard Andrews ◽  
Tse-Hwei Choo ◽  
...  

2014 ◽  
Vol 24 (2) ◽  
pp. 305-314 ◽  
Author(s):  
Cicely Kerr ◽  
Katie Breheny ◽  
Andrew Lloyd ◽  
John Brazier ◽  
Donald B. Bailey ◽  
...  

2017 ◽  
Vol 5 (S2) ◽  
pp. AB010-AB010
Author(s):  
Tri Winarni ◽  
Tanjung Sumekar ◽  
Widodo Sardjana ◽  
Hardian Hardian ◽  
Sultana MH Faradz

Author(s):  
Randi Hagerman ◽  
Julie Lauterborn ◽  
Jacky Au ◽  
Elizabeth Berry-Kravis

2012 ◽  
Vol 2012 ◽  
pp. 1-4 ◽  
Author(s):  
Tri Indah Winarni ◽  
Andrea Schneider ◽  
Mariya Borodyanskara ◽  
Randi J. Hagerman

Fragile X syndrome (FXS) is the most common inherited cause of intellectual disability due to an expansion in the full mutation range (>200 CGG repeats) of the promoter region of theFMR1gene leading to gene silencing. Lack of FMRP, a critical protein for dendritic spine formation and maturation, will cause FXS. Early environmental enrichment combined with pharmacological intervention has been proven to rescue dendritic spine abnormalities in the animal model of FXS. Here we report on 2 young children with FXS who were treated early with a combination of targeted treatment and intensive educational interventions leading to improvement in their cognition and behavior and a normal IQ.


2017 ◽  
Vol 93 (2) ◽  
pp. 216-222 ◽  
Author(s):  
A.B.C. Dy ◽  
F. Tassone ◽  
M. Eldeeb ◽  
M.J. Salcedo-Arellano ◽  
N. Tartaglia ◽  
...  

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