Repetitive and ritualistic behaviour in children with Prader-Willi syndrome and children with autism

Background  Recent research has shown that the range of repetitive behaviour seen in individuals with Prader–Willi syndrome (PWS) extends beyond food‐related behaviour. Methods  The presence and intensity of repetitive, rigid and routinized behaviour in children with PWS was compared with that seen...

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Published inJournal of intellectual disability research Vol. 50; no. 2; pp. 92 - 100
Main Authors Greaves, N., Prince, E., Evans, D. W., Charman, T.
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Science Ltd 01.02.2006
Blackwell Publishing
Blackwell
Wiley Subscription Services, Inc
Subjects
Online AccessGet full text
ISSN0964-2633
1365-2788
DOI10.1111/j.1365-2788.2005.00726.x

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Abstract Background  Recent research has shown that the range of repetitive behaviour seen in individuals with Prader–Willi syndrome (PWS) extends beyond food‐related behaviour. Methods  The presence and intensity of repetitive, rigid and routinized behaviour in children with PWS was compared with that seen in children with another neurodevelopmental condition in which repetitive behaviour is common: children with autism. Parents completed the Childhood Routines Inventory (CRI). Results  Contrary to our predictions, controlling for developmental level, children with PWS and children with autism showed similar levels of repetitive and ritualistic behaviour overall and on the two CRI factors measuring ‘just right’ and ‘repetitive’ behaviour. Indeed, the majority of the sample of parents of children with PWS endorsed most items on the CRI. However there was some specificity at the level of individual items with parents of children with PWS more frequently endorsing an item on ‘collecting and storing objects’ and parents of children with autism more frequently endorsing ‘lining up objects’, ‘has a strong preference for certain foods’ and ‘seems aware of detail at home’. Conclusions  These findings confirm the range of repetitive behaviours that form part of the behavioural phenotype of PWS, including insistence on sameness and ‘just right’ behaviours, and uncover a surprising overlap with those seen in children with autism. Clinical management for children with PWS should include advice and education regarding management of repetitive and rigid behaviour. Future research should investigate whether the repetitive behaviours that form part of the behavioural phenotype of both PWS and autism are associated with a common neuropsychological, neurotransmitter or genetic origin.
AbstractList Recent research has shown that the range of repetitive behaviour seen in individuals with Prader-Willi syndrome (PWS) extends beyond food-related behaviour. The presence and intensity of repetitive, rigid and routinized behaviour in children with PWS was compared with that seen in children with another neurodevelopmental condition in which repetitive behaviour is common: children with autism. Parents completed the Childhood Routines Inventory (CRI). Contrary to our predictions, controlling for developmental level, children with PWS and children with autism showed similar levels of repetitive and ritualistic behaviour overall and on the two CRI factors measuring 'just right' and 'repetitive' behaviour. Indeed, the majority of the sample of parents of children with PWS endorsed most items on the CRI. However there was some specificity at the level of individual items with parents of children with PWS more frequently endorsing an item on 'collecting and storing objects' and parents of children with autism more frequently endorsing 'lining up objects', 'has a strong preference for certain foods' and 'seems aware of detail at home'. These findings confirm the range of repetitive behaviours that form part of the behavioural phenotype of PWS, including insistence on sameness and 'just right' behaviours, and uncover a surprising overlap with those seen in children with autism. Clinical management for children with PWS should include advice and education regarding management of repetitive and rigid behaviour. Future research should investigate whether the repetitive behaviours that form part of the behavioural phenotype of both PWS and autism are associated with a common neuropsychological, neurotransmitter or genetic origin.
Background  Recent research has shown that the range of repetitive behaviour seen in individuals with Prader–Willi syndrome (PWS) extends beyond food‐related behaviour. Methods  The presence and intensity of repetitive, rigid and routinized behaviour in children with PWS was compared with that seen in children with another neurodevelopmental condition in which repetitive behaviour is common: children with autism. Parents completed the Childhood Routines Inventory (CRI). Results  Contrary to our predictions, controlling for developmental level, children with PWS and children with autism showed similar levels of repetitive and ritualistic behaviour overall and on the two CRI factors measuring ‘just right’ and ‘repetitive’ behaviour. Indeed, the majority of the sample of parents of children with PWS endorsed most items on the CRI. However there was some specificity at the level of individual items with parents of children with PWS more frequently endorsing an item on ‘collecting and storing objects’ and parents of children with autism more frequently endorsing ‘lining up objects’, ‘has a strong preference for certain foods’ and ‘seems aware of detail at home’. Conclusions  These findings confirm the range of repetitive behaviours that form part of the behavioural phenotype of PWS, including insistence on sameness and ‘just right’ behaviours, and uncover a surprising overlap with those seen in children with autism. Clinical management for children with PWS should include advice and education regarding management of repetitive and rigid behaviour. Future research should investigate whether the repetitive behaviours that form part of the behavioural phenotype of both PWS and autism are associated with a common neuropsychological, neurotransmitter or genetic origin.
Recent research has shown that the range of repetitive behaviour seen in individuals with Prader-Willi syndrome (PWS) extends beyond food-related behaviour.BACKGROUNDRecent research has shown that the range of repetitive behaviour seen in individuals with Prader-Willi syndrome (PWS) extends beyond food-related behaviour.The presence and intensity of repetitive, rigid and routinized behaviour in children with PWS was compared with that seen in children with another neurodevelopmental condition in which repetitive behaviour is common: children with autism. Parents completed the Childhood Routines Inventory (CRI).METHODSThe presence and intensity of repetitive, rigid and routinized behaviour in children with PWS was compared with that seen in children with another neurodevelopmental condition in which repetitive behaviour is common: children with autism. Parents completed the Childhood Routines Inventory (CRI).Contrary to our predictions, controlling for developmental level, children with PWS and children with autism showed similar levels of repetitive and ritualistic behaviour overall and on the two CRI factors measuring 'just right' and 'repetitive' behaviour. Indeed, the majority of the sample of parents of children with PWS endorsed most items on the CRI. However there was some specificity at the level of individual items with parents of children with PWS more frequently endorsing an item on 'collecting and storing objects' and parents of children with autism more frequently endorsing 'lining up objects', 'has a strong preference for certain foods' and 'seems aware of detail at home'.RESULTSContrary to our predictions, controlling for developmental level, children with PWS and children with autism showed similar levels of repetitive and ritualistic behaviour overall and on the two CRI factors measuring 'just right' and 'repetitive' behaviour. Indeed, the majority of the sample of parents of children with PWS endorsed most items on the CRI. However there was some specificity at the level of individual items with parents of children with PWS more frequently endorsing an item on 'collecting and storing objects' and parents of children with autism more frequently endorsing 'lining up objects', 'has a strong preference for certain foods' and 'seems aware of detail at home'.These findings confirm the range of repetitive behaviours that form part of the behavioural phenotype of PWS, including insistence on sameness and 'just right' behaviours, and uncover a surprising overlap with those seen in children with autism. Clinical management for children with PWS should include advice and education regarding management of repetitive and rigid behaviour. Future research should investigate whether the repetitive behaviours that form part of the behavioural phenotype of both PWS and autism are associated with a common neuropsychological, neurotransmitter or genetic origin.CONCLUSIONSThese findings confirm the range of repetitive behaviours that form part of the behavioural phenotype of PWS, including insistence on sameness and 'just right' behaviours, and uncover a surprising overlap with those seen in children with autism. Clinical management for children with PWS should include advice and education regarding management of repetitive and rigid behaviour. Future research should investigate whether the repetitive behaviours that form part of the behavioural phenotype of both PWS and autism are associated with a common neuropsychological, neurotransmitter or genetic origin.
Research to compare presence, intensity and pattern of repetitive behaviours in children with Prader-Willi syndrome with that in children with autism. Parents recruited via UK national organisations for the conditions were surveyed using the Childhood Routines Inventory. [(BNI unique abstract)] 44 references
Background  Recent research has shown that the range of repetitive behaviour seen in individuals with Prader–Willi syndrome (PWS) extends beyond food‐related behaviour. Methods  The presence and intensity of repetitive, rigid and routinized behaviour in children with PWS was compared with that seen in children with another neurodevelopmental condition in which repetitive behaviour is common: children with autism. Parents completed the Childhood Routines Inventory (CRI). Results  Contrary to our predictions, controlling for developmental level, children with PWS and children with autism showed similar levels of repetitive and ritualistic behaviour overall and on the two CRI factors measuring ‘just right’ and ‘repetitive’ behaviour. Indeed, the majority of the sample of parents of children with PWS endorsed most items on the CRI. However there was some specificity at the level of individual items with parents of children with PWS more frequently endorsing an item on ‘collecting and storing objects’ and parents of children with autism more frequently endorsing ‘lining up objects’, ‘has a strong preference for certain foods’ and ‘seems aware of detail at home’. Conclusions  These findings confirm the range of repetitive behaviours that form part of the behavioural phenotype of PWS, including insistence on sameness and ‘just right’ behaviours, and uncover a surprising overlap with those seen in children with autism. Clinical management for children with PWS should include advice and education regarding management of repetitive and rigid behaviour. Future research should investigate whether the repetitive behaviours that form part of the behavioural phenotype of both PWS and autism are associated with a common neuropsychological, neurotransmitter or genetic origin.
Background Recent research has shown that the range of repetitive behaviour seen in individuals with Prader-Willi syndrome (PWS) extends beyond food-related behaviour. Methods The presence and intensity of repetitive, rigid and routinized behaviour in children with PWS was compared with that seen in children with another neurodevelopmental condition in which repetitive behaviour is common: children with autism. Parents completed the Childhood Routines Inventory (CRI). Results Contrary to our predictions, controlling for developmental level, children with PWS and children with autism showed similar levels of repetitive and ritualistic behaviour overall and on the two CRI factors measuring 'just right' and 'repetitive' behaviour. Indeed, the majority of the sample of parents of children with PWS endorsed most items on the CRI. However there was some specificity at the level of individual items with parents of children with PWS more frequently endorsing an item on 'collecting and storing objects' and parents of children with autism more frequently endorsing 'lining up objects', 'has a strong preference for certain foods' and 'seems aware of detail at home'. Conclusions These findings confirm the range of repetitive behaviours that form part of the behavioural phenotype of PWS, including insistence on sameness and 'just right' behaviours, and uncover a surprising overlap with those seen in children with autism. Clinical management for children with PWS should include advice and education regarding management of repetitive and rigid behaviour. Future research should investigate whether the repetitive behaviours that form part of the behavioural phenotype of both PWS and autism are associated with a common neuropsychological, neurotransmitter or genetic origin. Tables, y, References. Adapted from the source document.
Recent research has shown that the range of repetitive behaviour seen in individuals with Prader-Willi syndrome (PWS) extends beyond food-related behaviour. The presence and intensity of repetitive, rigid and routinized behaviour in children with PWS was compared with that seen in children with another neurodevelopmental condition in which repetitive behaviour is common: children with autism. Parents completed the Childhood Routines Inventory (CRI). Contrary to our predictions, controlling for developmental level, children with PWS and children with autism showed similar levels of repetitive and ritualistic behaviour overall and on the two CRI factors measuring 'just right' and 'repetitive' behaviour. Indeed, the majority of the sample of parents of children with PWS endorsed most items on the CRI. However there was some specificity at the level of individual items with parents of children with PWS more frequently endorsing an item on 'collecting and storing objects' and parents of children with autism more frequently endorsing 'lining up objects', 'has a strong preference for certain foods' and 'seems aware of detail at home'. These findings confirm the range of repetitive behaviours that form part of the behavioural phenotype of PWS, including insistence on sameness and 'just right' behaviours, and uncover a surprising overlap with those seen in children with autism. Clinical management for children with PWS should include advice and education regarding management of repetitive and rigid behaviour. Future research should investigate whether the repetitive behaviours that form part of the behavioural phenotype of both PWS and autism are associated with a common neuropsychological, neurotransmitter or genetic origin.
Background: Recent research has shown that the range of repetitive behaviour seen in individuals with Prader-Willi syndrome (PWS) extends beyond food-related behaviour. Methods: The presence and intensity of repetitive, rigid and routinized behaviour in children with PWS was compared with that seen in children with another neurodevelopmental condition in which repetitive behaviour is common: children with autism. Parents completed the Childhood Routines Inventory (CRI). Results: Contrary to our predictions, controlling for developmental level, children with PWS and children with autism showed similar levels of repetitive and ritualistic behaviour overall and on the two CRI factors measuring just right and repetitive behaviour. Indeed, the majority of the sample of parents of children with PWS endorsed most items on the CRI. However there was some specificity at the level of individual items with parents of children with PWS more frequently endorsing an item on collecting and storing objects and parents of children with autism more frequently endorsing lining up objects, has a strong preference for certain foods and seems aware of detail at home. Conclusions: These findings confirm the range of repetitive behaviours that form part of the behavioural phenotype of PWS, including insistence on sameness and just right behaviours, and uncover a surprising overlap with those seen in children with autism. Clinical management for children with PWS should include advice and education regarding management of repetitive and rigid behaviour. Future research should investigate whether the repetitive behaviours that form part of the behavioural phenotype of both PWS and autism are associated with a common neuropsychological, neurotransmitter or genetic origin.
Author Evans, D. W.
Greaves, N.
Charman, T.
Prince, E.
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Issue 2
Keywords Endocrinopathy
Human
Preschool age
rigid behaviour
Diseases of the osteoarticular system
Clinical form
Developmental disorder
Rite
Genetic disease
Behavioral disorder
Autism
Symptomatology
School age
Behavioral analysis
repetitive behaviour
ritualistic behaviour
Adolescent
Severity score
Complex syndrome
Child
Prader Labhart Willi syndrome
Comparative study
Repetition
Prader-Willi syndrome (PWS)
Language English
License CC BY 4.0
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PublicationTitle Journal of intellectual disability research
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References Dimitropoulos A., Feurer I. D., Roof E., Stone W., Butler M. G., Sutcliffe J. & Thompson T. (2000) Appetite, behavior, compulsivity, and neurochemistry in Prader-Willi syndrome. Mental Retardation and Developmental Disabilities Research Reviews 6, 125-30.
World Health Organisation (1993) Mental Disorders: A Glossary and Guide to their Classification in Accordance with the 10th Revision of the International Classification of Diseases: Research Diagnostic Criteria (ICD-10). WHO, Geneva.
Carter A. S., Volkmar F. R., Sparrow S. S., Wang J. J., Lord C., Dawson G., Fombonne E., Loveland K., Mesibov G. & Schopler E. (1998) The vineland adaptive behavior scales: supplementary norms for individuals with autism. Journal of Autism and Developmental Disorders 28, 287-302.
McDougle C. J., Naylor S. T., Goodman W. K., Volkmar F. R., Cohen D. J. & Price L. H. (1993) Acute tryptophan depletion in autistic disorder: a controlled case study. Biological Psychiatry 33, 547-50.
Lewis M. H. & Bodfish J. W. (1998) Repetitive behavior disorders in autism. Mental Retardation and Developmental Disabilities Research Reviews 4, 80-9.
Dykens E. M., Cassidy S. B. & King B. H. (1999) Maladaptive behavior differences in Prader-Willi syndrome due to paternal deletion versus maternal uniparental disomy. American Journal on Mental Retardation 104, 67-77.
Goodman W. K., Price L. H., Rasmussen S. A., Mazure C., Delagado P., Heninger G. R. & Charney D. S. (1989b) The Yale-Brown Obsessive-Compulsive Scale (Y-BOCS): Part II. Alidity. Archives of General Psychiatry 46, 1012-6.
Dykens E. M., Leckman J. F. & Cassidy S. B. (1996) Obsessions and compulsions in Prader-Willi syndrome. Journal of Child Psychology and Psychiatry 37, 995-1002.
Sparrow S., Balla D. & Cicchetti D. (1984) Vineland Adaptive Behavior Scales. American Guidance Service, Circle Pines, MN.
Dykens E. M. & Hodapp R. M. (2001) Research in mental retardation: toward an etiologic approach. Journal of Child Psychology and Psychiatry 42, 49-71.
Horner R. H., Carr E. G., Strain P. S., Todd A. W. & Reed H. K. (2002) Problem behavior interventions for young children with autism: a research synthesis. Journal of Autism and Developmental Disorders 32, 423-46.
Gunay-Aygun M., Schwartz S., Heeger S., O'Riordan M. A. & Cassidy S. B. (2001) The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and proposed revised criteria. Pediatrics 108, e92.
Feurer I. D., Dimitropoulos A., Stone W. L., Roof E., Butler M. G. & Thompson T. (1998) The latent variable structure of the compulsive behavior checklist in people with Prader-Willi syndrome. Journal of Intellectual Disability Research 42, 472-80.
Wingren M. & Hansen S. (2003) Rituals and compulsivity in Prader-Willi syndrome: profile and stability. Journal of Intellectual Disability Research 47, 428-38.
Dykens E. M. & Cassidy S. B. (1995) Correlates of maladaptive behavior in children and adults with Prader-Willi Syndrome. American Journal of Medical Genetics 60, 546-9.
Roof E., Stone W., MacLean W., Feurer I. D., Thompson T. & Butler M. G. (2000) Intellectual characteristics of Prader-Willi syndrome: comparison of genetic subtypes. Journal of Intellectual Disability Research 44, 25-30.
Veltman M. W., Thompson R. J., Roberts S. E., Thomas N. S., Whittington J. & Bolton P. F. (2004) Prader-Willi syndrome: a study comparing deletion and uniparental disomy cases with reference to autism spectrum disorders. European Child and Adolescent Psychiatry 13, 42-50.
McDougle C. J., Kresch L., Goodman W. K., Naylor S. T., Volkmar F. R., Cohen D. J. & Price L. H. (1995) A case-controlled study of repetitive thoughts and behavior in adults with autistic disorder and obsessive-compulsive disorder. American Journal of Psychiatry 152, 772-7.
Goodman W. K., Price L. H., Rasmussen S. A., Mazure C., Fleischman R. L., Hill C. L., Heninger G. R. & Charney D. S. (1989a) The Yale-Brown Obsessive-Compulsive Scale (Y-BOCS): Part I. Development, use, and reliability. Archives of General Psychiatry 46, 1006-11.
Jacobsen J., King B. H., Leventhal B. L., Christian S. L., Ledbetter D. H. & Cook E. H. (1998) Molecular screening for proximal 15q abnormalities in a mentally retarded population. Journal of Medical Genetics 35, 534-8.
Benjamin E. & Buot-Smith T. (1993) Naltrexone and fluoxetine in Prader-Willi syndrome. Journal of the American Academy of Child and Adolescent Psychiatry 32, 870-3.
Gillberg C., Steffenburg S., Wahlstrom J., Gillberg I. C., Sjostedt A., Martinsson T., Liedgren S. & Eeg-Olofsson O. (1991) Autism associated with marker chromosome. Journal of the American Academy of Child and Adolescent Psychiatry 30, 489-94.
Turner M. (1999) Annotation: repetitive behavior in autism: a review of psychological research. Journal of Child Psychology and Psychiatry 40, 839-49.
Evans D. W., Leckman J. F., Carter A., Reznick J. S., Henshaw D., King R. A. & Pauls D. (1997) Ritual, habit and perfectionism: the prevalence and development of compulsive-like behavior in normal young children. Child Development 68, 58-68.
Whittington J. E., Holland A. J., Webb T., Butler J., Clarke D. & Boer H. (2002) Relationship between clinical and genetic diagnosis of Prader-Willi syndrome. Journal of Medical Genetics 39, 926-32.
Evans D. W. & Gray F. L. (2000) Compulsive-like behavior in individuals with Down syndrome: its relation to mental age level, adaptive and maladaptive behavior. Child Development 71, 288-300.
Chakrabarti S. & Fombonne E. (2001) Pervasive developmental disorders in preschool children. Journal of the American Medical Association 285, 3093-9.
Clarke D. J., Boer H., Whittington J., Holland A., Butler J. & Webb T. (2002) Prader-Willi syndrome, compulsive and ritualistic behaviours: the first population-based survey. British Journal of Psychiatry 180, 358-62.
Boer H., Holland A., Whittington J., Butler J., Webb T. & Clarke D. (2002) Psychotic illness in people with Prader Willi syndrome due to chromosome 15 maternal uniparental disomy. Lancet 359, 135-6.
Dykens E. M., Hodapp R. M., Walsh K. K. & Nash L. J. (1992) Adaptive and maladaptive behavior in Prader-Willi Syndrome. Journal of the American Academy of Child and Adolescent Psychiatry 31, 1131-6.
Fombonne E. (2003) Epidemiological surveys of autism and other pervasive developmental disorders: an update. Journal of Autism and Developmental Disorders 33, 365-82.
Whitman B. Y. & Accardo P. (1987) Emotional problems in Prader-Willi Syndrome adolescents. American Journal of Medical Genetics 28, 897-905.
Sparrow S. (2000) Vineland Adaptive Behavior Scales - Screener Manual. Yale University, Yale, MA.
Thomas J. A., Johnson J., Peterson Kraai T. L., Wilson R., Tartaglia N., LeRoux J., Beischel L., McGavran L. & Hagerman R. J. (2003) Genetic and clinical characterization of patients with an interstitial duplication 15q11-q13, emphasizing behavioral phenotype and response to treatment. American Journal of Medical Genetics 119A, 111-20.
Holm V. A., Cassidy S. B. & Butler M. G. (1993) Prader-Willi syndrome: consensus diagnostic criteria. Pediatrics 91, 398-402.
Shao Y., Cuccaro M. L., Hauser E. R. et al. (2003) Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes. American Journal of Human Genetics 72, 539-48.
Whittington J. & Holland T. (2004) Prader-Willi Syndrome: Development and Manifestations. Cambridge Universtity Press, Cambridge.
American Psychiatric Association (1994) Diagnostic and Statistical Manual of Mental Disorders, 4th edn. (DSM-IV). APA, Washington, DC.
Cook E. H., Rowlett R., Jaselkis C. & Leventhal B. L. (1992) Fluoxetine treatment of children and adults with autistic disorder and mental retardation. Journal of the American Academy of Child and Adolescent Psychiatry 31, 739-45.
Whittington J. E., Holland A. J., Webb T., Butler J., Clarke D. & Boer H. (2004) Cognitive abilities and genotype in a population-based sample of people with Prader-Willi syndrome. Journal of Intellectual Disability Research 48, 172-87.
Boer H. (2004) Behavioural Studies in Prader-Willi Syndrome. Maastricht University Press, Maastricht.
Holland A. J., Whittington J. E., Butler J., Webb T., Boer H. & Clarke D. (2003) Behavioural phenotypes associated with specific genetic disorders: evidence from a population-based study of people with Prader-Willi syndrome. Psychological Medicine 33, 141-53.
Charman T., Howlin P., Berry B. & Prince E. (2004) Measuring developmental progress of children with autism spectrum disorder on school entry using parent report. Autism: the International Journal of Research and Practice 8, 89-100.
2002; 39
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References_xml – reference: Roof E., Stone W., MacLean W., Feurer I. D., Thompson T. & Butler M. G. (2000) Intellectual characteristics of Prader-Willi syndrome: comparison of genetic subtypes. Journal of Intellectual Disability Research 44, 25-30.
– reference: American Psychiatric Association (1994) Diagnostic and Statistical Manual of Mental Disorders, 4th edn. (DSM-IV). APA, Washington, DC.
– reference: Thomas J. A., Johnson J., Peterson Kraai T. L., Wilson R., Tartaglia N., LeRoux J., Beischel L., McGavran L. & Hagerman R. J. (2003) Genetic and clinical characterization of patients with an interstitial duplication 15q11-q13, emphasizing behavioral phenotype and response to treatment. American Journal of Medical Genetics 119A, 111-20.
– reference: Sparrow S., Balla D. & Cicchetti D. (1984) Vineland Adaptive Behavior Scales. American Guidance Service, Circle Pines, MN.
– reference: Horner R. H., Carr E. G., Strain P. S., Todd A. W. & Reed H. K. (2002) Problem behavior interventions for young children with autism: a research synthesis. Journal of Autism and Developmental Disorders 32, 423-46.
– reference: Whittington J. E., Holland A. J., Webb T., Butler J., Clarke D. & Boer H. (2004) Cognitive abilities and genotype in a population-based sample of people with Prader-Willi syndrome. Journal of Intellectual Disability Research 48, 172-87.
– reference: Evans D. W. & Gray F. L. (2000) Compulsive-like behavior in individuals with Down syndrome: its relation to mental age level, adaptive and maladaptive behavior. Child Development 71, 288-300.
– reference: Whittington J. & Holland T. (2004) Prader-Willi Syndrome: Development and Manifestations. Cambridge Universtity Press, Cambridge.
– reference: Wingren M. & Hansen S. (2003) Rituals and compulsivity in Prader-Willi syndrome: profile and stability. Journal of Intellectual Disability Research 47, 428-38.
– reference: Shao Y., Cuccaro M. L., Hauser E. R. et al. (2003) Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes. American Journal of Human Genetics 72, 539-48.
– reference: Goodman W. K., Price L. H., Rasmussen S. A., Mazure C., Fleischman R. L., Hill C. L., Heninger G. R. & Charney D. S. (1989a) The Yale-Brown Obsessive-Compulsive Scale (Y-BOCS): Part I. Development, use, and reliability. Archives of General Psychiatry 46, 1006-11.
– reference: Dykens E. M., Cassidy S. B. & King B. H. (1999) Maladaptive behavior differences in Prader-Willi syndrome due to paternal deletion versus maternal uniparental disomy. American Journal on Mental Retardation 104, 67-77.
– reference: Cook E. H., Rowlett R., Jaselkis C. & Leventhal B. L. (1992) Fluoxetine treatment of children and adults with autistic disorder and mental retardation. Journal of the American Academy of Child and Adolescent Psychiatry 31, 739-45.
– reference: Dykens E. M. & Cassidy S. B. (1995) Correlates of maladaptive behavior in children and adults with Prader-Willi Syndrome. American Journal of Medical Genetics 60, 546-9.
– reference: Clarke D. J., Boer H., Whittington J., Holland A., Butler J. & Webb T. (2002) Prader-Willi syndrome, compulsive and ritualistic behaviours: the first population-based survey. British Journal of Psychiatry 180, 358-62.
– reference: Holm V. A., Cassidy S. B. & Butler M. G. (1993) Prader-Willi syndrome: consensus diagnostic criteria. Pediatrics 91, 398-402.
– reference: Carter A. S., Volkmar F. R., Sparrow S. S., Wang J. J., Lord C., Dawson G., Fombonne E., Loveland K., Mesibov G. & Schopler E. (1998) The vineland adaptive behavior scales: supplementary norms for individuals with autism. Journal of Autism and Developmental Disorders 28, 287-302.
– reference: Dykens E. M., Hodapp R. M., Walsh K. K. & Nash L. J. (1992) Adaptive and maladaptive behavior in Prader-Willi Syndrome. Journal of the American Academy of Child and Adolescent Psychiatry 31, 1131-6.
– reference: Gillberg C., Steffenburg S., Wahlstrom J., Gillberg I. C., Sjostedt A., Martinsson T., Liedgren S. & Eeg-Olofsson O. (1991) Autism associated with marker chromosome. Journal of the American Academy of Child and Adolescent Psychiatry 30, 489-94.
– reference: Dykens E. M. & Hodapp R. M. (2001) Research in mental retardation: toward an etiologic approach. Journal of Child Psychology and Psychiatry 42, 49-71.
– reference: Boer H., Holland A., Whittington J., Butler J., Webb T. & Clarke D. (2002) Psychotic illness in people with Prader Willi syndrome due to chromosome 15 maternal uniparental disomy. Lancet 359, 135-6.
– reference: Evans D. W., Leckman J. F., Carter A., Reznick J. S., Henshaw D., King R. A. & Pauls D. (1997) Ritual, habit and perfectionism: the prevalence and development of compulsive-like behavior in normal young children. Child Development 68, 58-68.
– reference: Feurer I. D., Dimitropoulos A., Stone W. L., Roof E., Butler M. G. & Thompson T. (1998) The latent variable structure of the compulsive behavior checklist in people with Prader-Willi syndrome. Journal of Intellectual Disability Research 42, 472-80.
– reference: Whitman B. Y. & Accardo P. (1987) Emotional problems in Prader-Willi Syndrome adolescents. American Journal of Medical Genetics 28, 897-905.
– reference: Holland A. J., Whittington J. E., Butler J., Webb T., Boer H. & Clarke D. (2003) Behavioural phenotypes associated with specific genetic disorders: evidence from a population-based study of people with Prader-Willi syndrome. Psychological Medicine 33, 141-53.
– reference: Chakrabarti S. & Fombonne E. (2001) Pervasive developmental disorders in preschool children. Journal of the American Medical Association 285, 3093-9.
– reference: Goodman W. K., Price L. H., Rasmussen S. A., Mazure C., Delagado P., Heninger G. R. & Charney D. S. (1989b) The Yale-Brown Obsessive-Compulsive Scale (Y-BOCS): Part II. Alidity. Archives of General Psychiatry 46, 1012-6.
– reference: Dykens E. M., Leckman J. F. & Cassidy S. B. (1996) Obsessions and compulsions in Prader-Willi syndrome. Journal of Child Psychology and Psychiatry 37, 995-1002.
– reference: Charman T., Howlin P., Berry B. & Prince E. (2004) Measuring developmental progress of children with autism spectrum disorder on school entry using parent report. Autism: the International Journal of Research and Practice 8, 89-100.
– reference: Whittington J. E., Holland A. J., Webb T., Butler J., Clarke D. & Boer H. (2002) Relationship between clinical and genetic diagnosis of Prader-Willi syndrome. Journal of Medical Genetics 39, 926-32.
– reference: Veltman M. W., Thompson R. J., Roberts S. E., Thomas N. S., Whittington J. & Bolton P. F. (2004) Prader-Willi syndrome: a study comparing deletion and uniparental disomy cases with reference to autism spectrum disorders. European Child and Adolescent Psychiatry 13, 42-50.
– reference: Fombonne E. (2003) Epidemiological surveys of autism and other pervasive developmental disorders: an update. Journal of Autism and Developmental Disorders 33, 365-82.
– reference: Gunay-Aygun M., Schwartz S., Heeger S., O'Riordan M. A. & Cassidy S. B. (2001) The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and proposed revised criteria. Pediatrics 108, e92.
– reference: McDougle C. J., Kresch L., Goodman W. K., Naylor S. T., Volkmar F. R., Cohen D. J. & Price L. H. (1995) A case-controlled study of repetitive thoughts and behavior in adults with autistic disorder and obsessive-compulsive disorder. American Journal of Psychiatry 152, 772-7.
– reference: Boer H. (2004) Behavioural Studies in Prader-Willi Syndrome. Maastricht University Press, Maastricht.
– reference: Lewis M. H. & Bodfish J. W. (1998) Repetitive behavior disorders in autism. Mental Retardation and Developmental Disabilities Research Reviews 4, 80-9.
– reference: Sparrow S. (2000) Vineland Adaptive Behavior Scales - Screener Manual. Yale University, Yale, MA.
– reference: Benjamin E. & Buot-Smith T. (1993) Naltrexone and fluoxetine in Prader-Willi syndrome. Journal of the American Academy of Child and Adolescent Psychiatry 32, 870-3.
– reference: Dimitropoulos A., Feurer I. D., Roof E., Stone W., Butler M. G., Sutcliffe J. & Thompson T. (2000) Appetite, behavior, compulsivity, and neurochemistry in Prader-Willi syndrome. Mental Retardation and Developmental Disabilities Research Reviews 6, 125-30.
– reference: World Health Organisation (1993) Mental Disorders: A Glossary and Guide to their Classification in Accordance with the 10th Revision of the International Classification of Diseases: Research Diagnostic Criteria (ICD-10). WHO, Geneva.
– reference: McDougle C. J., Naylor S. T., Goodman W. K., Volkmar F. R., Cohen D. J. & Price L. H. (1993) Acute tryptophan depletion in autistic disorder: a controlled case study. Biological Psychiatry 33, 547-50.
– reference: Turner M. (1999) Annotation: repetitive behavior in autism: a review of psychological research. Journal of Child Psychology and Psychiatry 40, 839-49.
– reference: Jacobsen J., King B. H., Leventhal B. L., Christian S. L., Ledbetter D. H. & Cook E. H. (1998) Molecular screening for proximal 15q abnormalities in a mentally retarded population. Journal of Medical Genetics 35, 534-8.
– volume: 91
  start-page: 398
  year: 1993
  end-page: 402
  article-title: Prader–Willi syndrome: consensus diagnostic criteria
  publication-title: Pediatrics
– volume: 108
  start-page: e92
  year: 2001
  article-title: The changing purpose of Prader–Willi syndrome clinical diagnostic criteria and proposed revised criteria
  publication-title: Pediatrics
– volume: 37
  start-page: 995
  year: 1996
  end-page: 1002
  article-title: Obsessions and compulsions in Prader–Willi syndrome
  publication-title: Journal of Child Psychology and Psychiatry
– volume: 48
  start-page: 172
  year: 2004
  end-page: 87
  article-title: Cognitive abilities and genotype in a population‐based sample of people with Prader–Willi syndrome
  publication-title: Journal of Intellectual Disability Research
– volume: 35
  start-page: 534
  year: 1998
  end-page: 8
  article-title: Molecular screening for proximal 15q abnormalities in a mentally retarded population
  publication-title: Journal of Medical Genetics
– volume: 33
  start-page: 547
  year: 1993
  end-page: 50
  article-title: Acute tryptophan depletion in autistic disorder: a controlled case study
  publication-title: Biological Psychiatry
– volume: 44
  start-page: 25
  year: 2000
  end-page: 30
  article-title: Intellectual characteristics of Prader–Willi syndrome: comparison of genetic subtypes
  publication-title: Journal of Intellectual Disability Research
– start-page: 325
  year: 1997
  end-page: 43
– volume: 30
  start-page: 489
  year: 1991
  end-page: 94
  article-title: Autism associated with marker chromosome
  publication-title: Journal of the American Academy of Child and Adolescent Psychiatry
– volume: 119A
  start-page: 111
  year: 2003
  end-page: 20
  article-title: Genetic and clinical characterization of patients with an interstitial duplication 15q11‐q13, emphasizing behavioral phenotype and response to treatment
  publication-title: American Journal of Medical Genetics
– volume: 39
  start-page: 926
  year: 2002
  end-page: 32
  article-title: Relationship between clinical and genetic diagnosis of Prader–Willi syndrome
  publication-title: Journal of Medical Genetics
– volume: 40
  start-page: 839
  year: 1999
  end-page: 49
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Snippet Background  Recent research has shown that the range of repetitive behaviour seen in individuals with Prader–Willi syndrome (PWS) extends beyond food‐related...
Background  Recent research has shown that the range of repetitive behaviour seen in individuals with Prader–Willi syndrome (PWS) extends beyond food‐related...
Background: Recent research has shown that the range of repetitive behaviour seen in individuals with Prader-Willi syndrome (PWS) extends beyond food-related...
Recent research has shown that the range of repetitive behaviour seen in individuals with Prader-Willi syndrome (PWS) extends beyond food-related behaviour....
Background Recent research has shown that the range of repetitive behaviour seen in individuals with Prader-Willi syndrome (PWS) extends beyond food-related...
Recent research has shown that the range of repetitive behaviour seen in individuals with Prader-Willi syndrome (PWS) extends beyond food-related...
Research to compare presence, intensity and pattern of repetitive behaviours in children with Prader-Willi syndrome with that in children with autism. Parents...
BACKGROUND: Recent research has shown that the range of repetitive behaviour seen in individuals with Prader-Willi syndrome (PWS) extends beyond food-related...
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StartPage 92
SubjectTerms Adolescent
Anxiety Disorders
Autism
Autism Spectrum Disorders
Autistic children
Autistic Disorder - diagnosis
Autistic Disorder - psychology
Behavior Modification
Behavior Patterns
Behavior Problems
Behavioral sciences
Biological and medical sciences
Ceremonial Behavior
Child
Child Behavior
Child clinical studies
Child, Preschool
Childhood
Children
Children & youth
Complex syndromes
Developmental Delays
Developmental disorders
Disabilities
Ethics
Female
Health care management
Humans
Infantile autism
Male
Medical genetics
Medical sciences
Neuropsychology
Obesity
Parents
Parents & parenting
Participant Characteristics
Personality Assessment
Prader-Willi syndrome
Prader-Willi syndrome (PWS)
Prader-Willi Syndrome - diagnosis
Prader-Willi Syndrome - psychology
Preferences
Psychology. Psychoanalysis. Psychiatry
Psychopathology. Psychiatry
Repetitive behaviour
Response Rates (Questionnaires)
rigid behaviour
ritualistic behaviour
Stereotyped Behavior
Surveys
Title Repetitive and ritualistic behaviour in children with Prader-Willi syndrome and children with autism
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