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 in | Journal of intellectual disability research Vol. 50; no. 2; pp. 92 - 100 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Oxford, UK
Blackwell Science Ltd
01.02.2006
Blackwell Publishing Blackwell Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
ISSN | 0964-2633 1365-2788 |
DOI | 10.1111/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. |
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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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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) |
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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. 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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 article-title: Annotation: repetitive behavior in autism: a review of psychological research publication-title: Journal of Child Psychology and Psychiatry – year: 2000 – volume: 28 start-page: 287 year: 1998 end-page: 302 article-title: The vineland adaptive behavior scales: supplementary norms for individuals with autism publication-title: Journal of Autism and Developmental Disorders – volume: 28 start-page: 897 year: 1987 end-page: 905 article-title: Emotional problems in Prader–Willi Syndrome adolescents publication-title: American Journal of Medical Genetics – volume: 13 start-page: 42 year: 2004 end-page: 50 article-title: Prader–Willi syndrome: a study comparing deletion and uniparental disomy cases with reference to autism spectrum disorders publication-title: European Child and Adolescent Psychiatry – volume: 33 start-page: 365 year: 2003 end-page: 82 article-title: Epidemiological surveys of autism and other pervasive developmental disorders: an update publication-title: Journal of Autism and Developmental Disorders – volume: 32 start-page: 423 year: 2002 end-page: 46 article-title: Problem behavior interventions for young children with autism: a research synthesis publication-title: Journal of Autism and Developmental Disorders – year: 1994 – volume: 180 start-page: 358 year: 2002 end-page: 62 article-title: Prader–Willi syndrome, compulsive and ritualistic behaviours: the first population‐based survey publication-title: British Journal of Psychiatry – volume: 32 start-page: 870 year: 1993 end-page: 3 article-title: Naltrexone and fluoxetine in Prader–Willi syndrome publication-title: Journal of the American Academy of Child and Adolescent Psychiatry – volume: 104 start-page: 67 year: 1999 end-page: 77 article-title: Maladaptive behavior differences in Prader–Willi syndrome due to paternal deletion versus maternal uniparental disomy publication-title: American Journal on Mental Retardation – volume: 42 start-page: 472 year: 1998 end-page: 80 article-title: The latent variable structure of the compulsive behavior checklist in people with Prader–Willi syndrome publication-title: Journal of Intellectual Disability Research – volume: 47 start-page: 428 year: 2003 end-page: 38 article-title: Rituals and compulsivity in Prader–Willi syndrome: profile and stability publication-title: Journal of Intellectual Disability Research – volume: 359 start-page: 135 year: 2002 end-page: 6 article-title: Psychotic illness in people with Prader Willi syndrome due to chromosome 15 maternal uniparental disomy publication-title: Lancet – year: 1984 – volume: 46 start-page: 1012 year: 1989b end-page: 6 article-title: The Yale‐Brown Obsessive‐Compulsive Scale (Y‐BOCS): Part II. Alidity publication-title: Archives of General Psychiatry – volume: 4 start-page: 80 year: 1998 end-page: 9 article-title: Repetitive behavior disorders in autism publication-title: Mental Retardation and Developmental Disabilities Research Reviews – volume: 46 start-page: 1006 year: 1989a end-page: 11 article-title: The Yale‐Brown Obsessive‐Compulsive Scale (Y‐BOCS): Part I. Development, use, and reliability publication-title: Archives of General Psychiatry – volume: 68 start-page: 58 year: 1997 end-page: 68 article-title: Ritual, habit and perfectionism: the prevalence and development of compulsive‐like behavior in normal young children publication-title: Child Development – volume: 72 start-page: 539 year: 2003 end-page: 48 article-title: Fine mapping of autistic disorder to chromosome 15q11‐q13 by use of phenotypic subtypes publication-title: American Journal of Human Genetics – volume: 42 start-page: 49 year: 2001 end-page: 71 article-title: Research in mental retardation: toward an etiologic approach publication-title: Journal of Child Psychology and Psychiatry – volume: 71 start-page: 288 year: 2000 end-page: 300 article-title: Compulsive‐like behavior in individuals with Down syndrome: its relation to mental age level, adaptive and maladaptive behavior publication-title: Child Development – year: 2004 – volume: 60 start-page: 546 year: 1995 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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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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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