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Gepubliceerd in: Journal of Autism and Developmental Disorders 8/2015

01-08-2015 | Original Paper

Mother–Child Interaction as a Window to a Unique Social Phenotype in 22q11.2 Deletion Syndrome and in Williams Syndrome

Auteurs: Omri Weisman, Ruth Feldman, Merav Burg-Malki, Miri Keren, Ronny Geva, Gil Diesendruck, Doron Gothelf

Gepubliceerd in: Journal of Autism and Developmental Disorders | Uitgave 8/2015

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Abstract

Mother-child interactions in 22q11.2 Deletion syndrome (22q11.2DS) and Williams syndrome (WS) were coded for maternal sensitivity/intrusiveness, child’s expression of affect, levels of engagement, and dyadic reciprocity. WS children were found to express more positive emotions towards their mothers compared to 22q11.2DS children and those with developmental delay in a conflict interaction. During the same interaction, dyads of 22q11.2DS children were characterized by higher levels of maternal intrusiveness, lower levels of child’s engagement and reduced reciprocity compared to dyads of typically developing children. Finally, 22q11.2DS children with the COMT Met allele showed less adaptive behaviors than children with the Val allele. Dyadic behaviors partially coincided with the distinct social phenotypes in these syndromes and are potential behavioral markers of psychopathological trajectory.
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Literatuur
go back to reference Angkustsiri, K., Goodlin-Jones, B., Deprey, L., Brahmbhatt, K., Harris, S., & Simon, T. J. (2014). Social impairments in chromosome 22q11. 2 deletion syndrome (22q11. 2DS): Autism spectrum disorder or a different endophenotype? Journal of Autism and Developmental Disorders, 44, 739–746.PubMedCentralPubMedCrossRef Angkustsiri, K., Goodlin-Jones, B., Deprey, L., Brahmbhatt, K., Harris, S., & Simon, T. J. (2014). Social impairments in chromosome 22q11. 2 deletion syndrome (22q11. 2DS): Autism spectrum disorder or a different endophenotype? Journal of Autism and Developmental Disorders, 44, 739–746.PubMedCentralPubMedCrossRef
go back to reference Antshel, K. M., Stallone, K., Abdulsabur, N., Shprintzen, R., Roizen, N., Higgins, A. M., & Kates, W. R. (2007). Temperament in velocardiofacial syndrome. Journal of Intellectual Disability Research, 51, 218–227.PubMedCrossRef Antshel, K. M., Stallone, K., Abdulsabur, N., Shprintzen, R., Roizen, N., Higgins, A. M., & Kates, W. R. (2007). Temperament in velocardiofacial syndrome. Journal of Intellectual Disability Research, 51, 218–227.PubMedCrossRef
go back to reference Bearden, C. E., Jawad, A. F., Lynch, D. R., Monterossso, J. R., Sokol, S., McDonald-McGinn, D. M., et al. (2005). Effects of COMT genotype on behavioral symptomatology in the 22q11. 2 Deletion Syndrome. Child Neuropsychology, 11(1), 109–117.PubMedCentralPubMedCrossRef Bearden, C. E., Jawad, A. F., Lynch, D. R., Monterossso, J. R., Sokol, S., McDonald-McGinn, D. M., et al. (2005). Effects of COMT genotype on behavioral symptomatology in the 22q11. 2 Deletion Syndrome. Child Neuropsychology, 11(1), 109–117.PubMedCentralPubMedCrossRef
go back to reference Bellugi, U., Adolphs, R., Cassady, C., & Chiles, M. (1999). Towards the neural basis for hypersociability in a genetic syndrome. NeuroReport, 10, 1653–1657.PubMedCrossRef Bellugi, U., Adolphs, R., Cassady, C., & Chiles, M. (1999). Towards the neural basis for hypersociability in a genetic syndrome. NeuroReport, 10, 1653–1657.PubMedCrossRef
go back to reference Debbané, M., Van der Linden, M., Glaser, B., & Eliez, S. (2010). Monitoring of self-generated speech in adolescents with 22q11.2 deletion syndrome. The British Journal of Clinical Psychology/The British Psychological Society, 49, 373–386.PubMedCrossRef Debbané, M., Van der Linden, M., Glaser, B., & Eliez, S. (2010). Monitoring of self-generated speech in adolescents with 22q11.2 deletion syndrome. The British Journal of Clinical Psychology/The British Psychological Society, 49, 373–386.PubMedCrossRef
go back to reference Delaherche, E., Chetouani, M., Mahdhaoui, A., Saint-Georges, C., Viaux, S., & Cohen, D. (2012). Interpersonal synchrony: A survey of evaluation methods across disciplines. IEEE Transactions on Affective Computing, 3(3), 349–365.CrossRef Delaherche, E., Chetouani, M., Mahdhaoui, A., Saint-Georges, C., Viaux, S., & Cohen, D. (2012). Interpersonal synchrony: A survey of evaluation methods across disciplines. IEEE Transactions on Affective Computing, 3(3), 349–365.CrossRef
go back to reference Doyle, T. F., Bellugi, U., Korenberg, J. R., & Graham, J. (2004). “Everybody in the world is my friend” hypersociability in young children with Williams syndrome. American Journal of Medical Genetics. Part A, 124A, 263–273.PubMedCrossRef Doyle, T. F., Bellugi, U., Korenberg, J. R., & Graham, J. (2004). “Everybody in the world is my friend” hypersociability in young children with Williams syndrome. American Journal of Medical Genetics. Part A, 124A, 263–273.PubMedCrossRef
go back to reference Drew, L. J., Crabtree, G. W., Markx, S., Stark, K. L., Chaverneff, F., Xu, B., et al. (2011). The 22q11. 2 microdeletion: Fifteen years of insights into the genetic and neural complexity of psychiatric disorders. International Journal of Developmental Neuroscience, 29, 259–281.PubMedCentralPubMedCrossRef Drew, L. J., Crabtree, G. W., Markx, S., Stark, K. L., Chaverneff, F., Xu, B., et al. (2011). The 22q11. 2 microdeletion: Fifteen years of insights into the genetic and neural complexity of psychiatric disorders. International Journal of Developmental Neuroscience, 29, 259–281.PubMedCentralPubMedCrossRef
go back to reference Dykens, E. M., & Rosner, B. A. (1999). Refining behavioral phenotypes: Personality-motivation in Williams and Prader–Willi syndromes. American Journal of Mental Retardation, 104, 158–169.PubMedCrossRef Dykens, E. M., & Rosner, B. A. (1999). Refining behavioral phenotypes: Personality-motivation in Williams and Prader–Willi syndromes. American Journal of Mental Retardation, 104, 158–169.PubMedCrossRef
go back to reference Feldman, R. (1998). Coding interactive behavior manual. Unpublished Manual; Bar-Ilan University, Israel. Feldman, R. (1998). Coding interactive behavior manual. Unpublished Manual; Bar-Ilan University, Israel.
go back to reference Feldman, R. (2007). Parent-infant synchrony: Biological foundations and developmental outcomes. Current Directions in Psychological Science, 16, 340–345.CrossRef Feldman, R. (2007). Parent-infant synchrony: Biological foundations and developmental outcomes. Current Directions in Psychological Science, 16, 340–345.CrossRef
go back to reference Feldman, R. (2010). The relational basis of adolescent adjustment: Trajectories of mother–child interactive behaviors from infancy to adolescence shape adolescents’ adaptation. Attachment & Human Development, 12(1–2), 173–192.CrossRef Feldman, R. (2010). The relational basis of adolescent adjustment: Trajectories of mother–child interactive behaviors from infancy to adolescence shape adolescents’ adaptation. Attachment & Human Development, 12(1–2), 173–192.CrossRef
go back to reference Feldman, R., Bamberger, E., & Kanat-Maymon, Y. (2013). Parent-specific reciprocity from infancy to adolescence shapes children’s social competence and dialogical skills. Attachment & Human Development, 15(4), 407–423.CrossRef Feldman, R., Bamberger, E., & Kanat-Maymon, Y. (2013). Parent-specific reciprocity from infancy to adolescence shapes children’s social competence and dialogical skills. Attachment & Human Development, 15(4), 407–423.CrossRef
go back to reference Feldman, R., & Eidelman, A. I. (2009). Biological and environmental initial conditions shape the trajectories of cognitive and social-emotional development across the first years of life. Developmental Science, 12(1), 194–200.PubMedCrossRef Feldman, R., & Eidelman, A. I. (2009). Biological and environmental initial conditions shape the trajectories of cognitive and social-emotional development across the first years of life. Developmental Science, 12(1), 194–200.PubMedCrossRef
go back to reference Feldman, R., Golan, O., Hirschler-Guttenberg, Y., Ostfeld-Etzion, S., & Zagoory-Sharon, O. (2014a). Parent–child interaction and oxytocin production in pre-schoolers with autism spectrum disorder. The British Journal of Psychiatry, 205(2), 107–112.PubMedCrossRef Feldman, R., Golan, O., Hirschler-Guttenberg, Y., Ostfeld-Etzion, S., & Zagoory-Sharon, O. (2014a). Parent–child interaction and oxytocin production in pre-schoolers with autism spectrum disorder. The British Journal of Psychiatry, 205(2), 107–112.PubMedCrossRef
go back to reference Feldman, R., & Masalha, S. (2010). Parent–child and triadic antecedents of children’s social competence: Cultural specificity, shared process. Developmental Psychology, 46(2), 455–467.PubMedCrossRef Feldman, R., & Masalha, S. (2010). Parent–child and triadic antecedents of children’s social competence: Cultural specificity, shared process. Developmental Psychology, 46(2), 455–467.PubMedCrossRef
go back to reference Feldman, R., Rosenthal, Z., & Eidelman, A. I. (2014b). Maternal-preterm skin-to-skin contact enhances child physiologic organization and cognitive control across the first 10 years of life. Biological Psychiatry, 75(1), 56–64.PubMedCrossRef Feldman, R., Rosenthal, Z., & Eidelman, A. I. (2014b). Maternal-preterm skin-to-skin contact enhances child physiologic organization and cognitive control across the first 10 years of life. Biological Psychiatry, 75(1), 56–64.PubMedCrossRef
go back to reference Golding-Kushner, K. J., Weller, G., & Shprintzen, R. J. (1985). Velo-cardio-facial syndrome: Language and psychological profiles. Journal of Craniofacial Genetics and Developmental Biology, 5, 259–266.PubMed Golding-Kushner, K. J., Weller, G., & Shprintzen, R. J. (1985). Velo-cardio-facial syndrome: Language and psychological profiles. Journal of Craniofacial Genetics and Developmental Biology, 5, 259–266.PubMed
go back to reference Gothelf, D. (2007). Velocardiofacial syndrome. Child and Adolescent Psychiatric Clinics of North America, 16(3), 677–693.PubMedCrossRef Gothelf, D. (2007). Velocardiofacial syndrome. Child and Adolescent Psychiatric Clinics of North America, 16(3), 677–693.PubMedCrossRef
go back to reference Gothelf, D., Eliez, S., Thompson, T., Hinard, C., Penniman, L., Feinstein, C., et al. (2005). COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11. 2 deletion syndrome. Nature Neuroscience, 8(11), 1500–1502.PubMedCrossRef Gothelf, D., Eliez, S., Thompson, T., Hinard, C., Penniman, L., Feinstein, C., et al. (2005). COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11. 2 deletion syndrome. Nature Neuroscience, 8(11), 1500–1502.PubMedCrossRef
go back to reference Gothelf, D., Feinstein, C., Thompson, T., Gur, E., Penniman, L., Van Stone, E., et al. (2007). Risk factors for the emergence of psychotic disorders in adolescents with 22q11. 2 deletion syndrome. American Journal of Psychiatry, 164(4), 663–669.PubMedCrossRef Gothelf, D., Feinstein, C., Thompson, T., Gur, E., Penniman, L., Van Stone, E., et al. (2007). Risk factors for the emergence of psychotic disorders in adolescents with 22q11. 2 deletion syndrome. American Journal of Psychiatry, 164(4), 663–669.PubMedCrossRef
go back to reference Gothelf, D., Law, A. J., Frisch, A., Chen, J., Zarchi, O., Michaelovsky, E., et al. (2014). Biological effects of COMT haplotypes and psychosis risk in 22q11. 2 deletion syndrome. Biological Psychiatry, 75(5), 406–413.PubMedCentralPubMedCrossRef Gothelf, D., Law, A. J., Frisch, A., Chen, J., Zarchi, O., Michaelovsky, E., et al. (2014). Biological effects of COMT haplotypes and psychosis risk in 22q11. 2 deletion syndrome. Biological Psychiatry, 75(5), 406–413.PubMedCentralPubMedCrossRef
go back to reference Gothelf, D., Schaer, M., & Eliez, S. (2008). Genes, brain development and psychiatric phenotypes in velo-cardio-facial syndrome. Developmental Disabilities Research Reviews, 14(1), 59–68.PubMedCrossRef Gothelf, D., Schaer, M., & Eliez, S. (2008). Genes, brain development and psychiatric phenotypes in velo-cardio-facial syndrome. Developmental Disabilities Research Reviews, 14(1), 59–68.PubMedCrossRef
go back to reference Green, T., Gothelf, D., Glaser, B., Debbane, M., Frisch, A., Kotler, M., et al. (2009). Psychiatric disorders and intellectual functioning throughout development in velocardiofacial (22q11.2 deletion) syndrome. Journal of the American Academy of Child and Adolescent Psychiatry, 48, 1060–1068.PubMedCrossRef Green, T., Gothelf, D., Glaser, B., Debbane, M., Frisch, A., Kotler, M., et al. (2009). Psychiatric disorders and intellectual functioning throughout development in velocardiofacial (22q11.2 deletion) syndrome. Journal of the American Academy of Child and Adolescent Psychiatry, 48, 1060–1068.PubMedCrossRef
go back to reference Hirschler-Guttenberg, Y., Golan, O., Ostfeld-Etzion, S., & Feldman, R. (2014). Mothering, fathering, and the regulation of negative and positive emotions in high-functioning preschoolers with autism spectrum disorder. Journal of Child Psychology and Psychiatry. doi:10.1111/jcpp.12311. Hirschler-Guttenberg, Y., Golan, O., Ostfeld-Etzion, S., & Feldman, R. (2014). Mothering, fathering, and the regulation of negative and positive emotions in high-functioning preschoolers with autism spectrum disorder. Journal of Child Psychology and Psychiatry. doi:10.​1111/​jcpp.​12311.
go back to reference Ho, J. S., Radoeva, P. D., Jalbrzikowski, M., Chow, C., Hopkins, J., Tran, W. C., et al. (2012). Deficits in mental state attributions in individuals with 22q11.2 deletion syndrome (velo-cardio-facial syndrome). Autism Research, 5, 407–418.PubMedCentralPubMedCrossRef Ho, J. S., Radoeva, P. D., Jalbrzikowski, M., Chow, C., Hopkins, J., Tran, W. C., et al. (2012). Deficits in mental state attributions in individuals with 22q11.2 deletion syndrome (velo-cardio-facial syndrome). Autism Research, 5, 407–418.PubMedCentralPubMedCrossRef
go back to reference Järvinen-Pasley, A., Bellugi, U., Reilly, J., Mills, D. L., Galaburda, A., Reiss, A. L., et al. (2008). Defining the social phenotype in Williams syndrome: A model for linking gene, the brain, and behavior. Development and Psychopathology, 20, 1–35.PubMedCentralPubMedCrossRef Järvinen-Pasley, A., Bellugi, U., Reilly, J., Mills, D. L., Galaburda, A., Reiss, A. L., et al. (2008). Defining the social phenotype in Williams syndrome: A model for linking gene, the brain, and behavior. Development and Psychopathology, 20, 1–35.PubMedCentralPubMedCrossRef
go back to reference Jones, W., Bellugi, U., Lai, Z., Chiles, M., Reilly, J., Lincoln, A., & Adolphs, R. (2000). Hypersociability in Williams syndrome. Journal of Cognitive Neuroscience, 12, 30–46.PubMedCrossRef Jones, W., Bellugi, U., Lai, Z., Chiles, M., Reilly, J., Lincoln, A., & Adolphs, R. (2000). Hypersociability in Williams syndrome. Journal of Cognitive Neuroscience, 12, 30–46.PubMedCrossRef
go back to reference Karayiorgou, M., Simon, T. J., & Gogos, J. A. (2010). 22q11. 2 microdeletions: Linking DNA structural variation to brain dysfunction and schizophrenia. Nature Reviews Neuroscience, 11(6), 402–416.PubMedCentralPubMedCrossRef Karayiorgou, M., Simon, T. J., & Gogos, J. A. (2010). 22q11. 2 microdeletions: Linking DNA structural variation to brain dysfunction and schizophrenia. Nature Reviews Neuroscience, 11(6), 402–416.PubMedCentralPubMedCrossRef
go back to reference Karmiloff-Smith, A., Broadbent, H., Farran, E. K., Longhi, E., D’Souza, D., Metcalfe, K., et al. (2012). Social cognition in Williams syndrome: Genotype/phenotype insights from partial deletion patients. Frontiers in Psychology, 3, 168.PubMedCentralPubMedCrossRef Karmiloff-Smith, A., Broadbent, H., Farran, E. K., Longhi, E., D’Souza, D., Metcalfe, K., et al. (2012). Social cognition in Williams syndrome: Genotype/phenotype insights from partial deletion patients. Frontiers in Psychology, 3, 168.PubMedCentralPubMedCrossRef
go back to reference Keren, M., Feldman, R., & Tyano, S. (2001). Diagnoses and interactive patterns of infants referred to a community-based infant mental health clinic. Journal of the American Academy of Child and Adolescent Psychiatry, 40, 27–35.PubMedCrossRef Keren, M., Feldman, R., & Tyano, S. (2001). Diagnoses and interactive patterns of infants referred to a community-based infant mental health clinic. Journal of the American Academy of Child and Adolescent Psychiatry, 40, 27–35.PubMedCrossRef
go back to reference Klein-Tasman, B. P., & Mervis, C. B. (2003). Distinctive personality characteristics of 8-, 9-, and 10-year-olds with Williams syndrome. Developmental Neuropsychology, 23, 269–290.PubMedCrossRef Klein-Tasman, B. P., & Mervis, C. B. (2003). Distinctive personality characteristics of 8-, 9-, and 10-year-olds with Williams syndrome. Developmental Neuropsychology, 23, 269–290.PubMedCrossRef
go back to reference Lachman, H. M., Papolos, D. F., Saito, T., Yu, Y. M., Szumlanski, C. L., & Weinshilboum, R. M. (1996). Human catechol-O-methyltransferase pharmacogenetics: Description of a functional polymorphism and its potential application to neuropsychiatric disorders. Pharmacogenetics, 6, 243–250.PubMedCrossRef Lachman, H. M., Papolos, D. F., Saito, T., Yu, Y. M., Szumlanski, C. L., & Weinshilboum, R. M. (1996). Human catechol-O-methyltransferase pharmacogenetics: Description of a functional polymorphism and its potential application to neuropsychiatric disorders. Pharmacogenetics, 6, 243–250.PubMedCrossRef
go back to reference Leclère, C., Viaux, S., Avril, M., Achard, C., Chetouani, M., Missonnier, S., & Cohen, D. (2014). Why synchrony matters during mother–child interactions: A systematic review. PLoS ONE, 9(12), e113571.PubMedCentralPubMedCrossRef Leclère, C., Viaux, S., Avril, M., Achard, C., Chetouani, M., Missonnier, S., & Cohen, D. (2014). Why synchrony matters during mother–child interactions: A systematic review. PLoS ONE, 9(12), e113571.PubMedCentralPubMedCrossRef
go back to reference Leyfer, O. T., Folstein, S. E., Bacalman, S., Davis, N. O., Dinh, E., Morgan, J., et al. (2006). Comorbid psychiatric disorders in children with autism: Interview development and rates of disorders. Journal of Autism and Developmental Disorders, 36(7), 849–861.PubMedCrossRef Leyfer, O. T., Folstein, S. E., Bacalman, S., Davis, N. O., Dinh, E., Morgan, J., et al. (2006). Comorbid psychiatric disorders in children with autism: Interview development and rates of disorders. Journal of Autism and Developmental Disorders, 36(7), 849–861.PubMedCrossRef
go back to reference Losh, M., Bellugi, U., & Anderson, J. D. (2001). Narrative as a social engagement tool: The excessive use of evaluation in narratives from children with Williams syndrome. Narrative Inquiry, 10(2), 265–290.CrossRef Losh, M., Bellugi, U., & Anderson, J. D. (2001). Narrative as a social engagement tool: The excessive use of evaluation in narratives from children with Williams syndrome. Narrative Inquiry, 10(2), 265–290.CrossRef
go back to reference Ly, T. M., & Hodapp, R. M. (2005). Children with Prader–Willi syndrome vs. Williams syndrome: Indirect effects on parents during a jigsaw puzzle task. Journal of Intellectual Disability Research, 49, 929–939.PubMedCrossRef Ly, T. M., & Hodapp, R. M. (2005). Children with Prader–Willi syndrome vs. Williams syndrome: Indirect effects on parents during a jigsaw puzzle task. Journal of Intellectual Disability Research, 49, 929–939.PubMedCrossRef
go back to reference Martens, M. A., Wilson, S. J., & Reutens, D. C. (2008). Research Review: Williams syndrome: A critical review of the cognitive, behavioral, and neuroanatomical phenotype. Journal of Child Psychology and Psychiatry, 49(6), 576–608.PubMedCrossRef Martens, M. A., Wilson, S. J., & Reutens, D. C. (2008). Research Review: Williams syndrome: A critical review of the cognitive, behavioral, and neuroanatomical phenotype. Journal of Child Psychology and Psychiatry, 49(6), 576–608.PubMedCrossRef
go back to reference Mervis, C. B. (2003). Williams syndrome: 15 years of psychological research. Developmental Neuropsychology, 23(1–2), 1–12.PubMedCrossRef Mervis, C. B. (2003). Williams syndrome: 15 years of psychological research. Developmental Neuropsychology, 23(1–2), 1–12.PubMedCrossRef
go back to reference Meyer-Lindenberg, A., Mervis, C. B., & Berman, K. F. (2006). Neural mechanisms in Williams syndrome: A unique window to genetic influences on cognition and behaviour. Nature Reviews Neuroscience, 7(5), 380–393.PubMedCrossRef Meyer-Lindenberg, A., Mervis, C. B., & Berman, K. F. (2006). Neural mechanisms in Williams syndrome: A unique window to genetic influences on cognition and behaviour. Nature Reviews Neuroscience, 7(5), 380–393.PubMedCrossRef
go back to reference Monks, S., Niarchou, M., Davies, A. R., Walters, J. T., Williams, N., Owen, M. J., et al. (2014). Further evidence for high rates of schizophrenia in 22q11. 2 deletion syndrome. Schizophrenia Research, 153(1), 231–236.PubMedCrossRef Monks, S., Niarchou, M., Davies, A. R., Walters, J. T., Williams, N., Owen, M. J., et al. (2014). Further evidence for high rates of schizophrenia in 22q11. 2 deletion syndrome. Schizophrenia Research, 153(1), 231–236.PubMedCrossRef
go back to reference Morrow, B., Goldberg, R., Carlson, C., Gupta, R. D., Sirotkin, H., Collins, J., et al. (1995). Molecular definition of the 22q11 deletions in velo-cardio-facial syndrome. American Journal of Human Genetics, 56(6), 1391.PubMedCentralPubMed Morrow, B., Goldberg, R., Carlson, C., Gupta, R. D., Sirotkin, H., Collins, J., et al. (1995). Molecular definition of the 22q11 deletions in velo-cardio-facial syndrome. American Journal of Human Genetics, 56(6), 1391.PubMedCentralPubMed
go back to reference Pearlman-Avnion, S., & Eviatar, Z. (2001). Narrative analysis in developmental social and linguistic pathologies: Dissociation between emotional and informational language use. Brain and Cognition, 48(2–3), 494–499. Pearlman-Avnion, S., & Eviatar, Z. (2001). Narrative analysis in developmental social and linguistic pathologies: Dissociation between emotional and informational language use. Brain and Cognition, 48(2–3), 494–499.
go back to reference Pober, B. R. (2010). Williams–Beuren syndrome. New England Journal of Medicine, 362(3), 239–252.PubMedCrossRef Pober, B. R. (2010). Williams–Beuren syndrome. New England Journal of Medicine, 362(3), 239–252.PubMedCrossRef
go back to reference Reilly, J., Losh, M., Bellugi, U., & Wulfeck, B. (2004). “Frog, where are you?” Narratives in children with specific language impairment, early focal brain injury, and Williams syndrome. Brain and Language, 88, 229–247.PubMedCrossRef Reilly, J., Losh, M., Bellugi, U., & Wulfeck, B. (2004). “Frog, where are you?” Narratives in children with specific language impairment, early focal brain injury, and Williams syndrome. Brain and Language, 88, 229–247.PubMedCrossRef
go back to reference Rescorla, L. A. (2005). Assessment of young children using the Achenbach System of Empirically Based Assessment (ASEBA). Mental Retardation and Developmental Disabilities Research Reviews, 11(3), 226–237.PubMedCrossRef Rescorla, L. A. (2005). Assessment of young children using the Achenbach System of Empirically Based Assessment (ASEBA). Mental Retardation and Developmental Disabilities Research Reviews, 11(3), 226–237.PubMedCrossRef
go back to reference Robertson, S. B., & Ellis Weismer, S. (1999). Effects of treatment on linguistic and social skills in toddlers with delayed language development. Journal of Speech, Language, and Hearing Research, 42(5), 1234–1248.PubMedCrossRef Robertson, S. B., & Ellis Weismer, S. (1999). Effects of treatment on linguistic and social skills in toddlers with delayed language development. Journal of Speech, Language, and Hearing Research, 42(5), 1234–1248.PubMedCrossRef
go back to reference Schneider, M., Debbané, M., Bassett, A. S., Chow, E. W., Fung, W. L. A., van den Bree, M. B., et al. (2014). Psychiatric disorders from childhood to adulthood in 22q11. 2 deletion syndrome: Results from the international consortium on brain and behavior in 22q11. 2 deletion syndrome. American Journal of Psychiatry, 171(6), 627–639.PubMedCentralPubMedCrossRef Schneider, M., Debbané, M., Bassett, A. S., Chow, E. W., Fung, W. L. A., van den Bree, M. B., et al. (2014). Psychiatric disorders from childhood to adulthood in 22q11. 2 deletion syndrome: Results from the international consortium on brain and behavior in 22q11. 2 deletion syndrome. American Journal of Psychiatry, 171(6), 627–639.PubMedCentralPubMedCrossRef
go back to reference Schneider, M., Van der Linden, M., Glaser, B., Rizzi, E., Dahoun, S. P., Hinard, C., et al. (2012). Preliminary structure and predictive value of attenuated negative symptoms in 22q11. 2 deletion syndrome. Psychiatry Research, 196(2), 277–284.PubMedCrossRef Schneider, M., Van der Linden, M., Glaser, B., Rizzi, E., Dahoun, S. P., Hinard, C., et al. (2012). Preliminary structure and predictive value of attenuated negative symptoms in 22q11. 2 deletion syndrome. Psychiatry Research, 196(2), 277–284.PubMedCrossRef
go back to reference Schonherz, Y., Davidov, M., Knafo, A., Zilkha, H., Shoval, G., Zalsman, G., et al. (2014). Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome. Journal of Neurodevelopmental Disorders, 6(1), 3.PubMedCentralPubMedCrossRef Schonherz, Y., Davidov, M., Knafo, A., Zilkha, H., Shoval, G., Zalsman, G., et al. (2014). Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome. Journal of Neurodevelopmental Disorders, 6(1), 3.PubMedCentralPubMedCrossRef
go back to reference Set, E., Saez, I., Zhu, L., Houser, D. E., Myung, N., Zhong, S., et al. (2014). Dissociable contribution of prefrontal and striatal dopaminergic genes to learning in economic games. Proceedings of the National Academy of Sciences, 111(26), 9615–9620.CrossRef Set, E., Saez, I., Zhu, L., Houser, D. E., Myung, N., Zhong, S., et al. (2014). Dissociable contribution of prefrontal and striatal dopaminergic genes to learning in economic games. Proceedings of the National Academy of Sciences, 111(26), 9615–9620.CrossRef
go back to reference Smith, L. E., Greenberg, J. S., Seltzer, M. M., & Hong, J. (2008). Symptoms and behavior problems of adolescents and adults with autism: Effects of mother–child relationship quality, warmth, and praise. American Journal of Mental Retardation, 113(5), 387–402.PubMedCentralPubMedCrossRef Smith, L. E., Greenberg, J. S., Seltzer, M. M., & Hong, J. (2008). Symptoms and behavior problems of adolescents and adults with autism: Effects of mother–child relationship quality, warmth, and praise. American Journal of Mental Retardation, 113(5), 387–402.PubMedCentralPubMedCrossRef
go back to reference Sparrow, S. S., & Cicchetti, D. V. (1985). Diagnostic uses of the vineland adaptive behavior scales. Journal of Pediatric Psychology, 10, 215–225.PubMedCrossRef Sparrow, S. S., & Cicchetti, D. V. (1985). Diagnostic uses of the vineland adaptive behavior scales. Journal of Pediatric Psychology, 10, 215–225.PubMedCrossRef
go back to reference Spiker, D., Boyce, G. C., & Boyce, L. K. (2002). Parent–child interactions when young children have disabilities. International Review of Research in Mental Retardation, 25, 35–70.CrossRef Spiker, D., Boyce, G. C., & Boyce, L. K. (2002). Parent–child interactions when young children have disabilities. International Review of Research in Mental Retardation, 25, 35–70.CrossRef
go back to reference Stoddard, J., Takarae, Y., & Simon, T. J. (2012). A second look: No effect of the COMT Val158Met polymorphism on conflict adaptation in youth with chromosome 22q11. 2 deletion syndrome. Schizophrenia Research, 135(1), 202–203.PubMedCentralPubMedCrossRef Stoddard, J., Takarae, Y., & Simon, T. J. (2012). A second look: No effect of the COMT Val158Met polymorphism on conflict adaptation in youth with chromosome 22q11. 2 deletion syndrome. Schizophrenia Research, 135(1), 202–203.PubMedCentralPubMedCrossRef
go back to reference Sullivan, K., & Tager-Flusberg, H. (1999). Second-order belief attribution in Williams syndrome: Intact or impaired? American Journal of Mental Retardation, 104(6), 523–532.PubMedCentralPubMedCrossRef Sullivan, K., & Tager-Flusberg, H. (1999). Second-order belief attribution in Williams syndrome: Intact or impaired? American Journal of Mental Retardation, 104(6), 523–532.PubMedCentralPubMedCrossRef
go back to reference Swillen, A., Devriendt, K., Legius, E., Prinzie, P., Vogels, A., Ghesquière, P., et al. (1999). The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence. Genetic Counseling (Geneva, Switzerland), 10, 79–88. Swillen, A., Devriendt, K., Legius, E., Prinzie, P., Vogels, A., Ghesquière, P., et al. (1999). The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence. Genetic Counseling (Geneva, Switzerland), 10, 79–88.
Metagegevens
Titel
Mother–Child Interaction as a Window to a Unique Social Phenotype in 22q11.2 Deletion Syndrome and in Williams Syndrome
Auteurs
Omri Weisman
Ruth Feldman
Merav Burg-Malki
Miri Keren
Ronny Geva
Gil Diesendruck
Doron Gothelf
Publicatiedatum
01-08-2015
Uitgeverij
Springer US
Gepubliceerd in
Journal of Autism and Developmental Disorders / Uitgave 8/2015
Print ISSN: 0162-3257
Elektronisch ISSN: 1573-3432
DOI
https://doi.org/10.1007/s10803-015-2425-6

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