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01-09-2007 | Artikelen

Neuropsychologische kenmerken van kinderen en adolescenten met een (lichte) verstandelijke beperking

Profielen in relatie tot etiologie

Auteurs: Ger J. A. Ramakers, Albert J. G. B. Ponsioen

Gepubliceerd in: Kind en adolescent | Uitgave 3/2007

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Abstract

Ramakers, G. J. A., & Ponsioen, A. J. G. B. (2007). Neuropsychological characteristics of children and adolescents with (mild) mental retardation. Profiles in relation to etiology, Kind en Adolescent, 28 (3), 119-134.
Neuropsychological assessment has demonstrated that different syndromic forms of intellectual disability, in addition to a global deficiency in cognitive functioning, can be characterized by a specific pattern of stronger and weaker abilities. In this article we describe findings obtained in neuropsychological studies of children and adolescents with borderline and mild mental retardation, and of several syndromic forms of mental retardation. Knowledge of the cognitive profile of individuals with intellectual disability can be used to generate more directed, evidence-based support which should promote the functioning and wellbeing of the person involved. From a developmental perspective, significant gains could be attained, in particular with children and adolescents with borderline and mild mental retardation.
Keywords: mild mental retardation, syndromes, neuropsychology.
Literatuur
go back to reference American Psychiatric Association (2000). Diagnostic and statistical manual of mental disorders, 4th edition, text revision ( dsm-iv-tr ). Washington, dc: American Psychiatric Association. American Psychiatric Association (2000). Diagnostic and statistical manual of mental disorders, 4th edition, text revision ( dsm-iv-tr ). Washington, dc: American Psychiatric Association.
go back to reference Atkinson, J., Braddick, O., Anker, S., Curran, W., Andrew, R., Wattam-Bell, J., & Braddick, F. (2003). Neurobiological models of visuospatial cognition in children with Williams syndrome: measures of dorsal-stream and frontal function. Developmental Neuropsychology, 23, 139-172.CrossRefPubMed Atkinson, J., Braddick, O., Anker, S., Curran, W., Andrew, R., Wattam-Bell, J., & Braddick, F. (2003). Neurobiological models of visuospatial cognition in children with Williams syndrome: measures of dorsal-stream and frontal function. Developmental Neuropsychology, 23, 139-172.CrossRefPubMed
go back to reference Bellugi, U., Marks, S., & Bihrle, A. (1988). Dissociation between language and cognitive functions in Williams syndrome. In D. Bishop, & K. Mogford (Eds.), Language development in exceptional circumstances (pp. 177-189). Edinburgh: Churchill Livingstone. Bellugi, U., Marks, S., & Bihrle, A. (1988). Dissociation between language and cognitive functions in Williams syndrome. In D. Bishop, & K. Mogford (Eds.), Language development in exceptional circumstances (pp. 177-189). Edinburgh: Churchill Livingstone.
go back to reference Bender, B. G., Linden, M. G., & Harmon, R. J. (2001). Neuropsychological and functional cognitive skills of 35 unselected adults with sex chromosome abnormalities. American Journal of Medical Genetics, 102, 309-313.CrossRefPubMed Bender, B. G., Linden, M. G., & Harmon, R. J. (2001). Neuropsychological and functional cognitive skills of 35 unselected adults with sex chromosome abnormalities. American Journal of Medical Genetics, 102, 309-313.CrossRefPubMed
go back to reference Bender, B. G., Linden, M. G., & Robinson, A. (1993). Neuropsychological impairment in 42 adolescents with sex chromosome abnormalities. American Journal of Medical Genetics, 48, 169-173.CrossRefPubMed Bender, B. G., Linden, M. G., & Robinson, A. (1993). Neuropsychological impairment in 42 adolescents with sex chromosome abnormalities. American Journal of Medical Genetics, 48, 169-173.CrossRefPubMed
go back to reference Carlesimo, G. A., Marotta, L., & Vicari, S. (1997). Long-term memory in mental retardation: evidence for a specific impairment in subjects with Down’s syndrome. Neuropsychologia, 35, 71-79.CrossRefPubMed Carlesimo, G. A., Marotta, L., & Vicari, S. (1997). Long-term memory in mental retardation: evidence for a specific impairment in subjects with Down’s syndrome. Neuropsychologia, 35, 71-79.CrossRefPubMed
go back to reference Chapman, R. S., & Hesketh, L. J. (2000). Behavioral phenotype of individuals with Down syndrome. Mental Retardation and Developmental Disability Research Reviews, 6, 84-95.CrossRef Chapman, R. S., & Hesketh, L. J. (2000). Behavioral phenotype of individuals with Down syndrome. Mental Retardation and Developmental Disability Research Reviews, 6, 84-95.CrossRef
go back to reference Chapman, R. S., Seung, H. K., Schwartz, S. E., & Kay-Raining Bird, E. (1998). Language skills of children and adolescents with Down syndrome: ii. Production deficits. Journal of Speech Language and Hearing Research, 41, 861-873. Chapman, R. S., Seung, H. K., Schwartz, S. E., & Kay-Raining Bird, E. (1998). Language skills of children and adolescents with Down syndrome: ii. Production deficits. Journal of Speech Language and Hearing Research, 41, 861-873.
go back to reference Cornish, K. M., Burack, J. A., Rahman, A., Munir, F., Russo, N., & Grant, C. (2005). Theory of mind deficits in children with fragile x syndrome. Journal of Intellectual Disability Research 49, 372-378.CrossRefPubMed Cornish, K. M., Burack, J. A., Rahman, A., Munir, F., Russo, N., & Grant, C. (2005). Theory of mind deficits in children with fragile x syndrome. Journal of Intellectual Disability Research 49, 372-378.CrossRefPubMed
go back to reference Cornish, K. M., Munir, F., & Cross, G. (1999). Spatial cognition in males with Fragile-x syndrome: evidence for a neuropsychological phenotype. Cortex, 35, 263-271.CrossRefPubMed Cornish, K. M., Munir, F., & Cross, G. (1999). Spatial cognition in males with Fragile-x syndrome: evidence for a neuropsychological phenotype. Cortex, 35, 263-271.CrossRefPubMed
go back to reference Cornish, K. M., Munir, F., & Cross G. (2001). Differential impact of the fmr-1 full mutation on memory and attention functioning: a neuropsychological perspective. Journal of Cognitive Neuroscience, 13, 144-150.CrossRefPubMed Cornish, K. M., Munir, F., & Cross G. (2001). Differential impact of the fmr-1 full mutation on memory and attention functioning: a neuropsychological perspective. Journal of Cognitive Neuroscience, 13, 144-150.CrossRefPubMed
go back to reference Cornish, K. M., Sudhalter, V., & Turk, J. (2004). Attention and language in fragile x. Mental Retardation and Developmental Disability Research Reviews, 10, 11-16.CrossRef Cornish, K. M., Sudhalter, V., & Turk, J. (2004). Attention and language in fragile x. Mental Retardation and Developmental Disability Research Reviews, 10, 11-16.CrossRef
go back to reference Cornish, K. M., Turk, J., Wilding, J., Sudhalter, V., Munir F., Kooy, F., & Hagerman, R. (2004). Annotation: Deconstructing the attention deficit in fragile x syndrome: a developmental neuropsychological approach. Journal of Child Psychology and Psychiatry, 45, 1042-1053.CrossRefPubMed Cornish, K. M., Turk, J., Wilding, J., Sudhalter, V., Munir F., Kooy, F., & Hagerman, R. (2004). Annotation: Deconstructing the attention deficit in fragile x syndrome: a developmental neuropsychological approach. Journal of Child Psychology and Psychiatry, 45, 1042-1053.CrossRefPubMed
go back to reference Culbertson, W. C., & Zilmer, E. A. (2005). Tower of London – Drexel University ( tol DX?TM ): 2 nd edition. Technical manual. North Tonawanda, ny: Multi-Health Systems Inc. Culbertson, W. C., & Zilmer, E. A. (2005). Tower of London – Drexel University ( tol DX?TM ): 2 nd edition. Technical manual. North Tonawanda, ny: Multi-Health Systems Inc.
go back to reference Curfs, L. M., Borghgraef, M., Wiegers, A., Schreppers-Tijdink, G. A., & Fryns, J. P. (1989). Strengths and weaknesses in the cognitive profile of fra(x) patients. Clinical Genetics, 36, 405-410.PubMed Curfs, L. M., Borghgraef, M., Wiegers, A., Schreppers-Tijdink, G. A., & Fryns, J. P. (1989). Strengths and weaknesses in the cognitive profile of fra(x) patients. Clinical Genetics, 36, 405-410.PubMed
go back to reference Curfs, L. M., Wiegers, A. M., Sommers, J. R., Borghgraef, M., & Fryns, J. P. (1991). Strengths and weaknesses in the cognitive profile of youngsters with Prader-Willi syndrome. Clinical Genetics, 40, 430-444.PubMed Curfs, L. M., Wiegers, A. M., Sommers, J. R., Borghgraef, M., & Fryns, J. P. (1991). Strengths and weaknesses in the cognitive profile of youngsters with Prader-Willi syndrome. Clinical Genetics, 40, 430-444.PubMed
go back to reference Dykens, E. M., Hodapp, R. M., & Evans, D. W. (1994). Profiles and development of adaptive behavior in children with Down syndrome. American Journal of Mental Retardation, 98, 580-587.PubMed Dykens, E. M., Hodapp, R. M., & Evans, D. W. (1994). Profiles and development of adaptive behavior in children with Down syndrome. American Journal of Mental Retardation, 98, 580-587.PubMed
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.CrossRefPubMed 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.CrossRefPubMed
go back to reference Fidler, D. J., Hepburn, S. L., Mankin, G., & Rogers, S. J. (2005). Praxis skills in young children with Down syndrome, other developmental disabilities, and typically developing children. American Journal of Occupational Therapy, 59, 129-138.PubMed Fidler, D. J., Hepburn, S. L., Mankin, G., & Rogers, S. J. (2005). Praxis skills in young children with Down syndrome, other developmental disabilities, and typically developing children. American Journal of Occupational Therapy, 59, 129-138.PubMed
go back to reference Fryns, J. P., Jacobs, J., Kleczkowska, A., & Van den Berghe, H. (1984). The psychological profile of the fragile x syndrome. Clinical Genetics, 25, 131-134.PubMedCrossRef Fryns, J. P., Jacobs, J., Kleczkowska, A., & Van den Berghe, H. (1984). The psychological profile of the fragile x syndrome. Clinical Genetics, 25, 131-134.PubMedCrossRef
go back to reference Geschwind, D. H., Boone, K. B., Miller, B. L., & Swerdloff, R. S. (2000). Neurobehavioral phenotype of Klinefelter syndrome. Mental Retardation and Developmental Disability Research Reviews, 6, 107-116.CrossRef Geschwind, D. H., Boone, K. B., Miller, B. L., & Swerdloff, R. S. (2000). Neurobehavioral phenotype of Klinefelter syndrome. Mental Retardation and Developmental Disability Research Reviews, 6, 107-116.CrossRef
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 Graham, J. M. Jr., Bashir, A. S., Stark, R. E., Silbert, A., & Walzer, S. (1988). Oral and written language abilities of xxy boys: implications for anticipatory guidance. Pediatrics, 81, 795-806.PubMed Graham, J. M. Jr., Bashir, A. S., Stark, R. E., Silbert, A., & Walzer, S. (1988). Oral and written language abilities of xxy boys: implications for anticipatory guidance. Pediatrics, 81, 795-806.PubMed
go back to reference Hatton, D. D., Wheeler, A. C., Skinner, M. L., Bailey, D. B., Sullivan, K. M., Roberts, J. E., Mirrett, P., & Clark, R. D. (2003). Adaptive behavior in children with fragile x syndrome. American Journal of Mental Retardation, 108, 373-390.CrossRefPubMed Hatton, D. D., Wheeler, A. C., Skinner, M. L., Bailey, D. B., Sullivan, K. M., Roberts, J. E., Mirrett, P., & Clark, R. D. (2003). Adaptive behavior in children with fragile x syndrome. American Journal of Mental Retardation, 108, 373-390.CrossRefPubMed
go back to reference Heaton, R. K., Chelune, G. J., Talley, J. L., Kay, G. G., & Curtis, G. (1993). Wisconsin Card Sorting Test manual. Revised and expended. Odessa: Psychological Assessment Resources. Heaton, R. K., Chelune, G. J., Talley, J. L., Kay, G. G., & Curtis, G. (1993). Wisconsin Card Sorting Test manual. Revised and expended. Odessa: Psychological Assessment Resources.
go back to reference Howlin, P., Davies, M., & Udwin, O. (1998). Cognitive functioning in adults with Williams syndrome. Journal of Child Psychology and Psychiatry, 39, 183-189.CrossRefPubMed Howlin, P., Davies, M., & Udwin, O. (1998). Cognitive functioning in adults with Williams syndrome. Journal of Child Psychology and Psychiatry, 39, 183-189.CrossRefPubMed
go back to reference Hyman, S. L., Shores, A., & North, K. N. (2005). The nature and frequency of cognitive deficits in children with neurofibromatosis type 1. Neurology, 65, 1037-1044.CrossRefPubMed Hyman, S. L., Shores, A., & North, K. N. (2005). The nature and frequency of cognitive deficits in children with neurofibromatosis type 1. Neurology, 65, 1037-1044.CrossRefPubMed
go back to reference Kogan, C. S., Boutet, I., Cornish, K., Zangenehpour, S., Mullen, K. T., Holden, J. J., Der Kaloustian, V. M., Andermann, E., & Chaudhuri, A. (2004). Differential impact of the fmr1 gene on visual processing in fragile x syndrome. Brain, 127, 591-601.CrossRefPubMed Kogan, C. S., Boutet, I., Cornish, K., Zangenehpour, S., Mullen, K. T., Holden, J. J., Der Kaloustian, V. M., Andermann, E., & Chaudhuri, A. (2004). Differential impact of the fmr1 gene on visual processing in fragile x syndrome. Brain, 127, 591-601.CrossRefPubMed
go back to reference Lanfranchi, S., Cornoldi, C., & Vianello, R. (2004). Verbal and visuospatial working memory deficits in children with Down syndrome. American Journal of Mental Retardation, 109, 456-466.CrossRefPubMed Lanfranchi, S., Cornoldi, C., & Vianello, R. (2004). Verbal and visuospatial working memory deficits in children with Down syndrome. American Journal of Mental Retardation, 109, 456-466.CrossRefPubMed
go back to reference Lesniak-Karpiak, K., Mazzocco, M. M., & Ross, J. L. (2003). Behavioral assessment of social anxiety in females with Turner or fragile x syndrome. Journal of Autism and Developmental Disorders, 33, 55-67.CrossRefPubMed Lesniak-Karpiak, K., Mazzocco, M. M., & Ross, J. L. (2003). Behavioral assessment of social anxiety in females with Turner or fragile x syndrome. Journal of Autism and Developmental Disorders, 33, 55-67.CrossRefPubMed
go back to reference Maes, B., Fryns, J. P., Van Walleghem, M., & Van den Berghe, H. (1993). Fragile-x syndrome and autism: a prevalent association or a misinterpreted connection? Genetic Counseling, 4, 245-263.PubMed Maes, B., Fryns, J. P., Van Walleghem, M., & Van den Berghe, H. (1993). Fragile-x syndrome and autism: a prevalent association or a misinterpreted connection? Genetic Counseling, 4, 245-263.PubMed
go back to reference Maes, B., Fryns, J. P., Van Walleghem, M., & Van den Berghe, H. (1994). Cognitive functioning and information processing of adult mentally retarded men with fragile-x syndrome. American Journal of Medical Genetics, 50, 190-200.CrossRefPubMed Maes, B., Fryns, J. P., Van Walleghem, M., & Van den Berghe, H. (1994). Cognitive functioning and information processing of adult mentally retarded men with fragile-x syndrome. American Journal of Medical Genetics, 50, 190-200.CrossRefPubMed
go back to reference Mattson, S. N., Calarco, K. E., & Lang, A. R. (2006). Focused and shifting attention in children with heavy prenatal alcohol exposure. Neuropsychology, 20, 361-369.CrossRefPubMed Mattson, S. N., Calarco, K. E., & Lang, A. R. (2006). Focused and shifting attention in children with heavy prenatal alcohol exposure. Neuropsychology, 20, 361-369.CrossRefPubMed
go back to reference Mattson, S. N., Goodman, A. M., Caine, C., Delis, D. C., & Riley, E. P. (1999). Executive functioning in children with heavy prenatal alcohol exposure. Alcoholism, Clinical and Experimental Research, 23, 1808-1815.PubMed Mattson, S. N., Goodman, A. M., Caine, C., Delis, D. C., & Riley, E. P. (1999). Executive functioning in children with heavy prenatal alcohol exposure. Alcoholism, Clinical and Experimental Research, 23, 1808-1815.PubMed
go back to reference Mattson, S. N., & Riley, E. P. (2000). Parent ratings of behavior in children with heavy prenatal alcohol exposure and iq-matched controls. Alcoholism, Clinical and Experimental Research, 24, 226-231.CrossRefPubMed Mattson, S. N., & Riley, E. P. (2000). Parent ratings of behavior in children with heavy prenatal alcohol exposure and iq-matched controls. Alcoholism, Clinical and Experimental Research, 24, 226-231.CrossRefPubMed
go back to reference Mazzocco, M. M. (2000). Advances in research on the fragile x syndrome. Mental Retardation and Developmental Disabililty Research Reviews, 6, 96-106.CrossRef Mazzocco, M. M. (2000). Advances in research on the fragile x syndrome. Mental Retardation and Developmental Disabililty Research Reviews, 6, 96-106.CrossRef
go back to reference Mazzocco, M. M., Singh Bhatia, N., & Lesniak-Karpiak, K. (2006). Visuospatial skills and their association with math performance in girls with fragile x or Turner syndrome. Child Neuropsychology, 12, 87-110.CrossRefPubMed Mazzocco, M. M., Singh Bhatia, N., & Lesniak-Karpiak, K. (2006). Visuospatial skills and their association with math performance in girls with fragile x or Turner syndrome. Child Neuropsychology, 12, 87-110.CrossRefPubMed
go back to reference Merrill, E. C. (2006). Interference and inhibition in tasks of selective attention by persons with and without mental retardation. American Journal of Mental Retardation, 111, 216-226.CrossRefPubMed Merrill, E. C. (2006). Interference and inhibition in tasks of selective attention by persons with and without mental retardation. American Journal of Mental Retardation, 111, 216-226.CrossRefPubMed
go back to reference Mervis, C. B., & Klein-Tasman, B. P. (2000). Williams syndrome: cognition, personality, and adaptive behavior. Mental Retardation and Developmental Disability Research Reviews, 6, 148-158.CrossRef Mervis, C. B., & Klein-Tasman, B. P. (2000). Williams syndrome: cognition, personality, and adaptive behavior. Mental Retardation and Developmental Disability Research Reviews, 6, 148-158.CrossRef
go back to reference Miller, J., Kranzler, J., Liu, Y., Schmalfuss, I., Theriaque, D. W., Shuster, J. J., Hatfield, A., Mueller, O. T., Goldstone, A. P., Sahoo, T., Beaudet, A. L., & Driscoll, D. J. (2006). Neurocognitive findings in Prader-Willi syndrome and early-onset morbid obesity. The Journal of Pediatrics, 149, 192-198.CrossRefPubMed Miller, J., Kranzler, J., Liu, Y., Schmalfuss, I., Theriaque, D. W., Shuster, J. J., Hatfield, A., Mueller, O. T., Goldstone, A. P., Sahoo, T., Beaudet, A. L., & Driscoll, D. J. (2006). Neurocognitive findings in Prader-Willi syndrome and early-onset morbid obesity. The Journal of Pediatrics, 149, 192-198.CrossRefPubMed
go back to reference Munir, F., Cornish, K. M., & Wilding, J. (2000). Nature of the working memory deficit in fragile-x syndrome. Brain and Cognition, 44, 387-401.CrossRefPubMed Munir, F., Cornish, K. M., & Wilding, J. (2000). Nature of the working memory deficit in fragile-x syndrome. Brain and Cognition, 44, 387-401.CrossRefPubMed
go back to reference Paterson, S. J., Girelli, L., Butterworth, B., & Karmiloff-Smith, A. (2006). Are numerical impairments syndrome specific? Evidence from Williams syndrome and Down’s syndrome. Journal of Child Psychology and Psychiatry, 47, 190-204.CrossRefPubMed Paterson, S. J., Girelli, L., Butterworth, B., & Karmiloff-Smith, A. (2006). Are numerical impairments syndrome specific? Evidence from Williams syndrome and Down’s syndrome. Journal of Child Psychology and Psychiatry, 47, 190-204.CrossRefPubMed
go back to reference Plesa-Skwerer, D., Faja, S., Schofield, C., Verbalis, A., & Tager-Flusberg, H. (2006). Perceiving facial and vocal expressions of emotion in individuals with Williams syndrome. American Journal of Mental Retardation, 111, 15-26.CrossRefPubMed Plesa-Skwerer, D., Faja, S., Schofield, C., Verbalis, A., & Tager-Flusberg, H. (2006). Perceiving facial and vocal expressions of emotion in individuals with Williams syndrome. American Journal of Mental Retardation, 111, 15-26.CrossRefPubMed
go back to reference Ponsioen, A. J. G. B. (2001). Cognitieve vaardigheden van licht verstandelijk gehandicapte kinderen en jongeren. Assen: Van Gorcum. Ponsioen, A. J. G. B. (2001). Cognitieve vaardigheden van licht verstandelijk gehandicapte kinderen en jongeren. Assen: Van Gorcum.
go back to reference Ponsioen, A., & Van der Molen, M. (2002). Cognitieve vaardigheden van licht verstandelijk gehandicapte kinderen en jongeren. Utrecht: ’s Heeren Loo. Ponsioen, A., & Van der Molen, M. (2002). Cognitieve vaardigheden van licht verstandelijk gehandicapte kinderen en jongeren. Utrecht: ’s Heeren Loo.
go back to reference Purser, H. R., & Jarrold, C. (2005). Impaired verbal short-term memory in Down syndrome reflects a capacity limitation rather than atypically rapid forgetting. Journal of Experimental Child Psychology, 91, 1-23.CrossRef Purser, H. R., & Jarrold, C. (2005). Impaired verbal short-term memory in Down syndrome reflects a capacity limitation rather than atypically rapid forgetting. Journal of Experimental Child Psychology, 91, 1-23.CrossRef
go back to 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.CrossRefPubMed 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.CrossRefPubMed
go back to reference Ropers, H. H., & Hamel, B. C. (2005). X-linked mental retardation. Nature Reviews Genetics, 6, 46-57.CrossRefPubMed Ropers, H. H., & Hamel, B. C. (2005). X-linked mental retardation. Nature Reviews Genetics, 6, 46-57.CrossRefPubMed
go back to reference Rovet, J., Netley, C., Keenan, M., Bailey, J., & Stewart, D. (1996). The psychoeducational profile of boys with Klinefelter syndrome. Journal of Learning Disabilities, 29, 180-196.CrossRefPubMed Rovet, J., Netley, C., Keenan, M., Bailey, J., & Stewart, D. (1996). The psychoeducational profile of boys with Klinefelter syndrome. Journal of Learning Disabilities, 29, 180-196.CrossRefPubMed
go back to reference Shprintzen, R. J. (2000). Velo-cardio-facial syndrome: a distinctive behavioral phenotype. Mental Retardation and Developmental Disabilities Research Reviews, 6, 142-147.CrossRefPubMed Shprintzen, R. J. (2000). Velo-cardio-facial syndrome: a distinctive behavioral phenotype. Mental Retardation and Developmental Disabilities Research Reviews, 6, 142-147.CrossRefPubMed
go back to reference Spanjaard, H., & Slot, W. (1999). Competentievergroting in de residentiële jeugdzorg. Baarn: Intro. Spanjaard, H., & Slot, W. (1999). Competentievergroting in de residentiële jeugdzorg. Baarn: Intro.
go back to reference Stoll, J., Bruinsma, W., & Konijn, C. (2003). Nieuwe cliënten voor Bureau Jeugdzorg? Jeugdigen met meervoudige problemen waaronder een lichte verstandelijke beperking en instrumenten voor herkenning en signalering. Utrecht: nizw. Stoll, J., Bruinsma, W., & Konijn, C. (2003). Nieuwe cliënten voor Bureau Jeugdzorg? Jeugdigen met meervoudige problemen waaronder een lichte verstandelijke beperking en instrumenten voor herkenning en signalering. Utrecht: nizw.
go back to reference Sullivan, K., Winner, E., & Tager-Flusberg, H. (2003). Can adolescents with Williams syndrome tell the difference between lies and jokes? Developmental Neuropsychology, 23, 85-103.CrossRefPubMed Sullivan, K., Winner, E., & Tager-Flusberg, H. (2003). Can adolescents with Williams syndrome tell the difference between lies and jokes? Developmental Neuropsychology, 23, 85-103.CrossRefPubMed
go back to reference Swillen, A., Devriendt, K., Legius, E., Eyskens, B., Dumoulin, M., Gewillig, M., & Fryns, D. (1997). Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 37 children and adolescents with vcfs. Journal of Medical Genetics, 34, 453-458.CrossRefPubMed Swillen, A., Devriendt, K., Legius, E., Eyskens, B., Dumoulin, M., Gewillig, M., & Fryns, D. (1997). Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 37 children and adolescents with vcfs. Journal of Medical Genetics, 34, 453-458.CrossRefPubMed
go back to reference Udwin, O., Davies, M., & Howlin, P. (1996). A longitudinal study of cognitive abilities and educational attainment in Williams syndrome. Developmental Medicine and Child Neurology, 38, 1020-1029.PubMed Udwin, O., Davies, M., & Howlin, P. (1996). A longitudinal study of cognitive abilities and educational attainment in Williams syndrome. Developmental Medicine and Child Neurology, 38, 1020-1029.PubMed
go back to reference Van den Wijngaard, M. & Ponsioen, A. J. G. B. (in voorbereiding). De relatie tussen Wechsler Intelligent Scale for Children, Cognitive Assessment System en Diagnostic Statistical Manual of Mental Disorders bij licht verstandelijk gehandicapte kinderen. Van den Wijngaard, M. & Ponsioen, A. J. G. B. (in voorbereiding). De relatie tussen Wechsler Intelligent Scale for Children, Cognitive Assessment System en Diagnostic Statistical Manual of Mental Disorders bij licht verstandelijk gehandicapte kinderen.
go back to reference Van Rijn, S., Swaab, H., Aleman, A., & Kahn, R. S. (2006). x Chromosomal effects on social cognitive processing and emotion regulation: A study with Klinefelter men (47, xxy). Schizophrenia Research, 84, 194-203.CrossRefPubMed Van Rijn, S., Swaab, H., Aleman, A., & Kahn, R. S. (2006). x Chromosomal effects on social cognitive processing and emotion regulation: A study with Klinefelter men (47, xxy). Schizophrenia Research, 84, 194-203.CrossRefPubMed
go back to reference Van Weelden, J. (1988). Moeilijk lerende kinderen. Rotterdam: Lemniscaat. Van Weelden, J. (1988). Moeilijk lerende kinderen. Rotterdam: Lemniscaat.
go back to reference Verhulst, F. C., Van der Ende, J., & Koot, H. M. (1996). Handleiding voor de cbcl /4-18. Rotterdam: Afdeling Kinder- en Jeugdpsychiatrie, Sophia Kinderziekenhuis, Erasmus Universiteit Rotterdam. Verhulst, F. C., Van der Ende, J., & Koot, H. M. (1996). Handleiding voor de cbcl /4-18. Rotterdam: Afdeling Kinder- en Jeugdpsychiatrie, Sophia Kinderziekenhuis, Erasmus Universiteit Rotterdam.
go back to reference Vicari, S., Bellucci, S., & Carlesimo, G. A. (2000). Implicit and explicit memory: a functional dissociation in persons with Down syndrome. Neuropsychologia, 38, 240-251.CrossRefPubMed Vicari, S., Bellucci, S., & Carlesimo, G. A. (2000). Implicit and explicit memory: a functional dissociation in persons with Down syndrome. Neuropsychologia, 38, 240-251.CrossRefPubMed
go back to reference Vicari, S., Bellucci, S., & Carlesimo, G. A. (2006). Evidence from two genetic syndromes for the independence of spatial and visual working memory. Developmental Medicine and Child Neurology, 48, 126-131.CrossRefPubMed Vicari, S., Bellucci, S., & Carlesimo, G. A. (2006). Evidence from two genetic syndromes for the independence of spatial and visual working memory. Developmental Medicine and Child Neurology, 48, 126-131.CrossRefPubMed
go back to reference Vicari, S., Carlesimo, A., & Caltagirone, C. (1995). Short-term memory in persons with intellectual disabilities and Down’s syndrome. Journal of Intellectual Disability Research, 39, 532-537.PubMedCrossRef Vicari, S., Carlesimo, A., & Caltagirone, C. (1995). Short-term memory in persons with intellectual disabilities and Down’s syndrome. Journal of Intellectual Disability Research, 39, 532-537.PubMedCrossRef
go back to reference Walley, R. M,. & Donaldson, M. D. (2005). An investigation of executive function abilities in adults with Prader-Willi syndrome. Journal of Intellectual Disability Research, 49, 613-625.CrossRefPubMed Walley, R. M,. & Donaldson, M. D. (2005). An investigation of executive function abilities in adults with Prader-Willi syndrome. Journal of Intellectual Disability Research, 49, 613-625.CrossRefPubMed
go back to reference Whittington, J., Holland, A., 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, 172-187.CrossRefPubMed Whittington, J., Holland, A., 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, 172-187.CrossRefPubMed
go back to reference Woodin, M., Wang, P. P., Aleman, D., McDonald-McGinn, D., Zackai, E., & Moss, E. (2001). Neuropsychological profile of children and adolescents with the 22q11.2 microdeletion. Genetics in Medicine, 3, 34-39.CrossRefPubMed Woodin, M., Wang, P. P., Aleman, D., McDonald-McGinn, D., Zackai, E., & Moss, E. (2001). Neuropsychological profile of children and adolescents with the 22q11.2 microdeletion. Genetics in Medicine, 3, 34-39.CrossRefPubMed
Metagegevens
Titel
Neuropsychologische kenmerken van kinderen en adolescenten met een (lichte) verstandelijke beperking
Profielen in relatie tot etiologie
Auteurs
Ger J. A. Ramakers
Albert J. G. B. Ponsioen
Publicatiedatum
01-09-2007
Uitgeverij
Bohn Stafleu van Loghum
Gepubliceerd in
Kind en adolescent / Uitgave 3/2007
Print ISSN: 0167-2436
Elektronisch ISSN: 1876-5998
DOI
https://doi.org/10.1007/BF03061025