Literature DB >> 10711647

Intellectual characteristics of Prader-Willi syndrome: comparison of genetic subtypes.

E Roof1, W Stone, W MacLean, I D Feurer, T Thompson, M G Butler.   

Abstract

Advances in genetics have led to an increased understanding of the role of the genotype on behavioural functioning. The purpose of the present study was to examine differences in intellectual functioning in individuals with Prader-Willi syndrome (PWS) with a paternal 15q11-q13 deletion versus maternal uniparental disomy (UPD) of chromosome 15. Measures of intelligence and academic achievement were administered to 38 individuals with PWS (24 with deletion and 14 with UPD). The subjects with UPD had significantly higher verbal IQ scores than those with deletion (P< 0.01). The magnitude of the difference in verbal IQ was 9.1 points (69.9 versus 60.8 for UPD and deletion PWS subjects, respectively). Only 17% of subjects with the 15q11-q13 deletion had a verbal IQ > or = 70, while 50% of those with UPD had a verbal IQ > or = 70. Performance IQ scores did not differ between the two PWS genetic subtype groups. This is the first report to document the difference between verbal and performance IQ score patterns among subjects with PWS of the deletion versus the UPD subtype.

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Year:  2000        PMID: 10711647      PMCID: PMC6790137          DOI: 10.1046/j.1365-2788.2000.00250.x

Source DB:  PubMed          Journal:  J Intellect Disabil Res        ISSN: 0964-2633


  31 in total

1.  Families of children with Prader-Willi syndrome: stress-support and relations to child characteristics.

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Journal:  J Autism Dev Disord       Date:  1997-02

Review 2.  Prader-Willi syndrome.

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4.  Prader-Willi Syndrome: Genetics and Behavior.

Authors:  Travis Thompson; Merlin G Butler; William E MacLean; Beth Joseph
Journal:  Peabody J Educ       Date:  1996

5.  Self-injurious behavior and Prader-Willi syndrome: behavioral forms and body locations.

Authors:  F J Symons; M G Butler; M D Sanders; I D Feurer; T Thompson
Journal:  Am J Ment Retard       Date:  1999-05

6.  Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15.

Authors:  S B Cassidy; M Forsythe; S Heeger; R D Nicholls; N Schork; P Benn; S Schwartz
Journal:  Am J Med Genet       Date:  1997-02-11

7.  Comparison of phenotype in uniparental disomy and deletion Prader-Willi syndrome: sex specific differences.

Authors:  J Mitchell; A Schinzel; S Langlois; G Gillessen-Kaesbach; S Schuffenhauer; R Michaelis; D Abeliovich; I Lerer; S Christian; M Guitart; D E McFadden; W P Robinson
Journal:  Am J Med Genet       Date:  1996-10-16

8.  Obsessive-compulsive disorder in mentally retarded patients.

Authors:  B Vitiello; S Spreat; D Behar
Journal:  J Nerv Ment Dis       Date:  1989-04       Impact factor: 2.254

9.  Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomy.

Authors:  A Mutirangura; F Greenberg; M G Butler; S Malcolm; R D Nicholls; A Chakravarti; D H Ledbetter
Journal:  Hum Mol Genet       Date:  1993-02       Impact factor: 6.150

Review 10.  Genomic imprinting and candidate genes in the Prader-Willi and Angelman syndromes.

Authors:  R D Nicholls
Journal:  Curr Opin Genet Dev       Date:  1993-06       Impact factor: 5.578

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  49 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

2.  Contributing factors of mortality in Prader-Willi syndrome.

Authors:  Jennifer Proffitt; Kathryn Osann; Barbara McManus; Virginia E Kimonis; Janalee Heinemann; Merlin G Butler; David A Stevenson; June-Anne Gold
Journal:  Am J Med Genet A       Date:  2018-12-19       Impact factor: 2.802

Review 3.  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

Review 4.  Prader-Willi syndrome and early-onset morbid obesity NIH rare disease consortium: A review of natural history study.

Authors:  Merlin G Butler; Virginia Kimonis; Elisabeth Dykens; June A Gold; Jennifer Miller; Roy Tamura; Daniel J Driscoll
Journal:  Am J Med Genet A       Date:  2017-12-22       Impact factor: 2.802

5.  The neuroanatomy of genetic subtype differences in Prader-Willi syndrome.

Authors:  Robyn A Honea; Laura M Holsen; Rebecca J Lepping; Rodrigo Perea; Merlin G Butler; William M Brooks; Cary R Savage
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2012-03       Impact factor: 3.568

6.  Prader-Willi Syndrome: Clinical and Genetic Findings.

Authors:  Merlin G Butler; Travis Thompson
Journal:  Endocrinologist       Date:  2000-07

7.  Genetic subtype differences in neural circuitry of food motivation in Prader-Willi syndrome.

Authors:  L M Holsen; J R Zarcone; R Chambers; M G Butler; D C Bittel; W M Brooks; T I Thompson; C R Savage
Journal:  Int J Obes (Lond)       Date:  2008-12-02       Impact factor: 5.095

8.  Clinical management of behavioral characteristics of Prader-Willi syndrome.

Authors:  Alan Y Ho; Anastasia Dimitropoulos
Journal:  Neuropsychiatr Dis Treat       Date:  2010-05-06       Impact factor: 2.570

9.  Prader-Willi syndrome.

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

Review 10.  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
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