Literature DB >> 11944876

Are jigsaw puzzle skills 'spared' in persons with Prader-Willi syndrome?

Elisabeth M Dykens1.   

Abstract

BACKGROUND: This three-part study examines previous clinical impressions that people with Prader-Willi syndrome have unusual jigsaw puzzle and word search skills.
RESULTS: Children with Prader-Willi syndrome showed relative strengths on standardized visual-spatial tasks (Object Assembly, Triangles, VMI) in that their scores were significantly higher than age- and IQ-matched peers with mixed mental retardation, but below those of age-matched normal children with average IQs. In striking contrast, children with Prader-Willi syndrome scored on par with normal peers on word searches, and they far outperformed them on the jigsaw puzzles, placing more than twice as many pieces as the typically-developing group. Within Prader-Willi syndrome, puzzle proficiency was not predicted by age, IQ, gender, degree of obesity, or obsessive-compulsive symptoms, but by genetic subtypes of this disorder.
CONCLUSIONS: Findings are discussed in relation to splinter skills in autism, and to cases with autism and chromosome 15 anomalies that include the Prader-Willi region.

Entities:  

Mesh:

Year:  2002        PMID: 11944876     DOI: 10.1111/1469-7610.00025

Source DB:  PubMed          Journal:  J Child Psychol Psychiatry        ISSN: 0021-9630            Impact factor:   8.982


  23 in total

1.  Microarray analysis of gene/transcript expression in Angelman syndrome: deletion versus UPD.

Authors:  Douglas C Bittel; Nataliya Kibiryeva; Zohreh Talebizadeh; Daniel J Driscoll; Merlin G Butler
Journal:  Genomics       Date:  2005-01       Impact factor: 5.736

Review 2.  Prader-Willi Syndrome - Clinical Genetics, Diagnosis and Treatment Approaches: An Update.

Authors:  Merlin G Butler; Jennifer L Miller; Janice L Forster
Journal:  Curr Pediatr Rev       Date:  2019

3.  Comparison of perinatal factors in deletion versus uniparental disomy in Prader-Willi syndrome.

Authors:  June-Anne Gold; Ranim Mahmoud; Suzanne B Cassidy; Virginia Kimonis
Journal:  Am J Med Genet A       Date:  2018-05       Impact factor: 2.802

4.  Methylation-specific multiplex ligation-dependent probe amplification and identification of deletion genetic subtypes in Prader-Willi syndrome.

Authors:  Rebecca S Henkhaus; Soo-Jeong Kim; Virginia E Kimonis; June-Anne Gold; Elisabeth M Dykens; Daniel J Driscoll; Merlin G Butler
Journal:  Genet Test Mol Biomarkers       Date:  2011-10-06

5.  Leisure activities in Prader-Wili syndrome: implications for health, cognition and adaptive functioning.

Authors:  Elisabeth M Dykens
Journal:  J Autism Dev Disord       Date:  2014-02

6.  Prader-Willi syndrome.

Authors:  Suzanne B Cassidy; Daniel J Driscoll
Journal:  Eur J Hum Genet       Date:  2008-09-10       Impact factor: 4.246

Review 7.  Prader-Willi Syndrome: Clinical Genetics and Diagnostic Aspects with Treatment Approaches.

Authors:  Merlin G Butler; Ann M Manzardo; Janice L Forster
Journal:  Curr Pediatr Rev       Date:  2016

Review 8.  Studying interactions, reactions, and perceptions: can genetic disorders serve as behavioral proxies?

Authors:  Robert M Hodapp
Journal:  J Autism Dev Disord       Date:  2004-02

9.  Microarray analysis of gene/transcript expression in Prader-Willi syndrome: deletion versus UPD.

Authors:  D C Bittel; N Kibiryeva; Z Talebizadeh; M G Butler
Journal:  J Med Genet       Date:  2003-08       Impact factor: 6.318

Review 10.  Single Gene and Syndromic Causes of Obesity: Illustrative Examples.

Authors:  Merlin G Butler
Journal:  Prog Mol Biol Transl Sci       Date:  2016-03-23       Impact factor: 3.622

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