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CASE REPORT

Autism and Williams syndrome: A case report

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Pages 186-188 | Received 21 Sep 2005, Published online: 12 Jul 2009

References

  • Bellugi U, Lichtenberger L, Mills D, Galaburda A, Korenberg JR. Bridging cognition, the brain and the molecular genetics: Evidence from Williams syndrome. Trends Neurosci 1999; 22: 197–207
  • Curran ME, Atkinson DL, Ewart AK, Morris CA, Leppert MF, Keating MT. The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosis. Cell 1993; 73: 159–168
  • American Psychiatric Association. 1994. Diagnostic and statistical manual of mental disorders. 4th ed. Washington, DC: American Psychiatric Association Press.
  • Donnai D, Karmiloff-Smith A. Williams syndrome; From genotype through to the cognitive phenotype. Am J Med Genet 2000; 97: 164–171
  • Gillberg, C, Coleman, M. 2000. The biology of the autistic syndromes. 3rd ed. London: MacKeith Press ( distributed by Cambridge University Press).
  • Gillberg C, Rasmussen P. Brief report: Four case histories and a literature review of Williams syndrome and autistic behavior. J Autism Dev Disord 1994; 24: 381–393
  • Gosch A, Pankau R. Autistic behavior in two children with Williams-Beuren syndrome. Am J Med Genet 1994; 53: 83–84
  • Jones W, Bellugi U, Lai Z, Chiles M, Reilly J, Lincoln A, Adolphs R. Hypersociability in Williams syndrome. J Cogn Neurosci Suppl 2000; 1: 30–46
  • Kielinen M, Rantala H, Timonen E, Linna SL, Moilanen I. Associated medical disorders and disabilities in children with autistic disorder: a population-based study. Autism 2004; 8: 49–60
  • Krug DA, Arick J, Almond P. Behavior checklist for identifying severely handicapped individuals with high levels of autistic behavior. J Child Psychol Psychiatry 1980; 21: 221–229
  • Laws G, Bishop D. Pragmatic language impairment and social deficits in Williams syndrome: A comparison with Down's syndrome and specific language impairment. Int J Lang Commun Disord 2004; 39: 45–64
  • Meng X, Lu X, Li Z, Green ED, Massa H, Trask BJ, Morris CA, Keating MT. Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel gene. Hum Genet 1998; 103: 590–599
  • Muhle R, Trentacoste SV, Rapin I. The genetics of autism. Pediatrics 2004; 113: 472–486
  • Osborne LR. Williams-Beuren syndrome: unraveling the mysteries of a microdeletion disorder. Mol Genet Metab 1999; 67: 1–10
  • Peterson BS, Panksepp J. Biological basis of childhood neuropsychiatric disorders. Textbook of biological psychiatry, J Panksepp. Wiley-Liss, New York 2004; 393–436
  • Pober BR, Dykens EM. Williams syndrome: An overview of medical, clinical and behavioral features. Child Adolesc Psychiatr Clin North Am 1996; 5: 929–943
  • Reiss AL, Feinstein C, Rosenbaum KN, Borengasser-Caruso MA. Autism associated with Williams syndrome. Pediatrics 1985; 106: 247–249
  • Schopler E, Reichler RJ, DeVellis RF, Daly K. Toward objective classification of childhood autism: Childhood autism rating scale (CARS). J Autism Dev Disord 1980; 10: 91–103
  • Wu YQ, Sutton VR, Nickerson E, Lupski JR, Potocki L, Korenberg JR, Greenberg F, Tassabehji M, Shaffer LG. Delineation of the common critical region in Williams syndrome and clinical correlation of growth, heart defects, ethnicity, and parental origin. Am J Med Genet 1998; 78: 82–89

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