Comorbidity and diagnosis of developmental disorders

Current Issues in Developmental Disorders

Volumn , Issue , 2012, Pages 19-45

  Williams, David M ^a   Lind, Sophie E ^a  

^a DURHAM UNIVERSITY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 84879503620     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.4324/9780203100288     Document Type: Chapter

References (105)

1. Alarcon, M., Abrahams, B. S., Stone, J. L., Duvall, J. A., Perederiy, J. V., Bomar, J. M., Geschwind, D. H. (2008). Linkage, association and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene. American Journal of Human Genetics, 82, 150-159.
2. American Psychiatric Association. (2000). Diagnostic and Statistical Manual of Mental Disorders (4th ed., text revised). Washington DC: American Psychiatric Association.
3. American Psychiatric Association (2011). American Psychiatric Association DSM-5 development. A 09 autism spectrum disorder > Proposed revisions. Retrieved from http:// www.dsm5.org/ProposedRevisions/Pages/proposedrevision.aspx?rid=94#
4. Anderson, J. C., Williams, S., McGee, R., & Silva, P. A. (1987). DSM-III disorders in preadolescent children: Prevalence in a large sample from the general-population. Archives of General Psychiatry, 44, 69-76.
5. Arking, D. E., Cutler, D. J., Brune, C. W., Teslovich, T. M., West, K., Ikeda, M., Chakravarti, A. (2008). A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. American Journal of Human Genetics, 82, 160-164.
6. Baddeley, A., Gathercole, S. E., & Papagno, C. (1998). The phonological loop as a language learning device. Psychological Review, 105, 158-173.
7. Bailey, A., Le Couteur, A. Gottesman, I., Bolton, P., Simonoff, E., Yuzda, E., & Rutter, M. (1995). Autism as a strongly genetic disorder: Evidence from a British twin study. Psychological Medicine, 25, 63-77.
8. Baird, G., Simonoff, E., Pickles, A., Chandler, S., Loucas, T., Meldrum, D., & Charman T. (2006). Prevalence of disorders of the autism spectrum in a population cohort of children in South Thames: The Special Needs and Autism Project (SNAP). Lancet, 368, 210-215.
9. Barry, J. G., Yasin, I., & Bishop, D. V. M. (2007). Heritable risk factors associated with language impairments. Genes, Brain and Behavior, 6, 66-76.
10. Bental, B., & Tirosh, E. (2008). The effects of methylphenidate on word decoding accuracy in boys with attention-defi cit/hyperactivity disorder. Journal of Clinical Psychopharmacology, 28, 89-92.
11. Berument, S. K., Rutter, M., Lord, C., Pickles, A., & Bailey, A. (1999). Autism screening questionnaire: Diagnostic validity. The British Journal of Psychiatry, 175, 444-451.
12. Bishop, D. V. M. (2001). Genetic infl uences on language impairment and literacy problems in children: Same or different? Journal of Child Psychology and Psychiatry, 42, 189-198.
13. Bishop, D. V. M. (2006). Developmental cognitive genetics: How psychology can inform genetics. Quarterly Journal of Experimental Psychology, 59, 1153-1168.
14. Bishop, D. V. M. (2010). Overlaps between autism and language impairment: Phenomimicry or shared etiology? Behavior Genetics, 40, 618-629.
15. Bishop, D. V. M. (2011). Are our 'gold standard' autism diagnostic instruments fi t for purpose? [Web log message] Retrieved May 30, 2011, from http://deevybee.blogspot. com/2011/05/are-our-gold-standard-autism-diagnostic.html
16. Bishop, D. V. M., & Edmundson, A. (1987). Specifi c language impairment as a maturational lag: Evidence from longitudinal data on language and motor development. Developmental Medicine and Child Neurology, 29, 442-459.
17. Bishop, D. V. M., Maybery, M., Wong, D., Maley, A., Hill, W., & Hallmayer, J. (2004). Are phonological processing defi cits part of the broad autism phenotype? American Journal of Medical Genetics Part B-Neuropsychiatric Genetics, 128B(1), 54-60.
18. Bishop, D. V. M., North, T., & Donlan, C. (1995). Genetic basis of specifi c language impairment: Evidence from a twin study. Developmental Medicine and Child Neurology, 37, 56-71.
19. Botting, N. (2005). Non-verbal cognitive development and language impairment. Journal of Child Psychology and Psychiatry, 46, 317-326.
20. Butcher, L. M., Kennedy, J. K. J., & Plomin, R. (2006). Generalist genes and cognitive neuroscience. Current Opinion in Neurobiology, 16, 145-151.
21. Cardon, L. R., Smith, S. D., Fulker, D. W., Kimberling, W. J., Pennington, B. F., & DeFries, J. C. (1994). Quantitative trait locus for reading-disability on chromosome-6. Science 266, 276-279.
22. Constantino, J. N. (2002). The Social Responsiveness Scale. Los Angeles, CA: Western Psychological Services.
23. Constantino, J. N., & Todd, R. D. (2003). Autistic traits in the general population: A twin study. Archives of General Psychiatry, 60, 524-530.
24. Conti-Ramsden, G., Botting, N., & Faragher, B. (2001). Psycholinguistic markers for specifi c language impairment (SLI). Journal of Child Psychology and Psychiatry, 42, 741-748.
25. Conti-Ramsden, G., Falcaro, M., Simkin, Z., & Pickles, A. (2007). Familial loading in specifi c language impairment: Patterns of differences across proband characteristics, gender and relative type. Genes Brain and Behavior, 6, 216-228.
26. Cope, N., Harold, D., Hill, G., Moskvina, V., Stevenson, J., Holmans, P., Williams, J. (2005). Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia. American Journal of Human Genetics, 76, 581-591.
27. Costello, E. J., Farmer, E. M. Z., Angold, A., Burns, B. J., & Erkanli, A. (1997). Psychiatric disorders among American Indian and white youth in Appalachia: The Great Smoky Mountains Study. American Journal of Public Health, 87, 827-832.
28. Couto, J. M., Gomez, L., Wigg, K., Ickowicz, A., Pathare, T., Malone, M., Barr, C. L. (2009). Association of attention-defi cit/hyperactivity disorder with a candidate region for reading disabilities on chromosome 6p. Biological Psychiatry, 66, 368-375.
29. DeFries, J. C., & Fulker, D. W. (1985). Multiple-regression analysis of twin data. Behavior Genetics, 15, 467-473.
30. DeFries, J. C., & Fulker, D. W. (1988). Multiple-regression analysis of twin data: Etiology of deviant scores versus individual-differences. Acta Geneticae Medicae et Gemellologiae, 37, 205-216.
31. DeFries, J. C., Fulker, D. W., & LaBuda, M. C. (1987). Evidence for a genetic etiology in reading-disability of twins. Nature, 329, 537-539.
32. Dworzynski, K., A., Ronald, A., Hayiou-Thomas, M. E., McEwan, F., Happé, F., Bolton, P., & Plomin, R. (2008). Developmental path between language and autistic-like impairments: A twin study. Infant and Child Development, 17, 121-136.
33. Eaves, L. C., & Ho, H. H. (2004). The very early identifi cation of autism: Outcome to age 4½-5. Journal of Autism and Developmental Disorders, 34, 367-378.
34. Faraone, S. V., Perlis, R. H., Doyle, A. E., Smoller, J. W., Goralnick, J. J., Holmgren, M. A., & Sklar, P. (2005). Molecular genetics of attention-defi cit/hyperactivity disorder. Biological Psychiatry, 57, 1313-1323.
35. Feinstein, A. R. (1970). The pre-therapeutic classifi cation of co-morbidity in chronic disease. Journal of Chronic Disease, 23, 455-468.
36. Frangiskakis, J. M., Ewart, A. K., Morris, C. A., Mervis, C. B., Bertrand, J., Robinson, B. F., Keating, M. T. (1996). LIM-kinase1 hemizygosity implicated in impaired visuospatial constructive cognition. Cell, 86, 59-69.
37. Friedman, M. C., Chhabildas, N., Budhiraja, N., Willcutt, E. G., & Pennington, B. F. (2003). Etiology of the comorbidity between RD and ADHD: Exploration of the nonrandom mating hypothesis. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics, 120B, 109-115.
38. Gathercole, S. E., & Baddeley, A. D. (1990). Phonological memory defi cits in language disordered children: Is there a causal connection? Journal of Memory and Language, 29, 336-360.
39. Gau, S. S., & Shang, C. (2010). Executive functions as endophenotypes in ADHD: Evidence from the Cambridge Neuropsychological Test Battery (CANTAB). Journal of Child Psychology and Psychiatry, 51, 838-849.
40. Gayan, J., Willcutt, E. G., Fisher, S. E., Francks, C., Cardon, L. R., Olson, R. K., DeFries, J. C. (2005). Bivariate linkage scan for reading disability and attention-defi - cit/hyperactivity disorder localizes pleiotropic loci. Journal of Child Psychology and Psychiatry, 46, 1045-1056.
41. Goodman, R. (1997). The Strengths and Diffi culties Questionnaire. Journal of Child Psychology and Psychiatry, 38, 581-586.
42. Gottesman, I. I., & Gould, T. D. (2003). The endophenotype concept in psychiatry: Etymology and strategic intentions. American Journal of Psychiatry, 160, 636-645.
43. Harold, D., Paracchini, S., Scerri, T., Dennis, M., Cope, N., Hill, G., Monaco, A. P. (2006). Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia. Molecular Psychiatry, 11, 1085-1091.
44. Hatcher, P. J., & Hulme, C. (1999). Phonemes, rhymes, and intelligence as predictors of children's responsiveness to remedial reading instruction: Evidence from a longitudinal intervention study. Journal of Experimental Child Psychology, 72, 130-153.
45. Jorde, L. B, Mason-Brothers, A., Waldmann, R., Ritvo, E. R., Freeman, B. J., Pingree, C., Mo, A. (1990). The UCLA University of Utah epidemiologic survey of autism: Genealogical analysis of familial aggregation. American Journal of Medical Genetics, 36, 85-88.
46. Karmiloff-Smith, A. (2008). Research into Williams Syndrome: The state of the art. In C. A. Nelson & M. Luciana (Eds.), Handbook of developmental cognitive neuroscience (pp. 691-700). Cambridge, MA: MIT Press.
47. Keulers, E. H. H., Hendriksen, J. G. M., Feron, F. J. M., Wassenberg, R., Wuisman-Frerker, M. G. F., Jolles, J., & Vles, S. H. (2007). Methylphenidate improves reading performance in children with attention defi cit hyperactivity disorder and comorbid dyslexia: An unblinded clinical trial. European Journal of Paediatric Neurology, 11, 21-28.
48. Kjelgaard, M. M., & Tager-Flusberg, H. (2001). An investigation of language impairment in autism: Implications for genetic subgroups. Language and Cognitive Processes, 16, 287-308.
49. LeCouteur, A., Lord, C., & Rutter, M. (2003). The Autism Diagnostic Interview - Revised (ADI-R). Los Angeles, CA: Western Psychological Services.
50. Leonard, L. B. (2000). Children with specifi c language impairment. Cambridge, MA: MIT Press.
51. Lindgren, K. A., Folstein, S. E., Tomblin, J. B., & Tager-Flusberg, H. (2009). Language and reading abilities of children with autism spectrum disorders and specifi c language impairment and their fi rst-degree relatives. Autism Research, 2, 22-38.
52. Lord, C., Risi, S., Lambrecht, L., Cook, E., Leventhal, B., DiLavore, B., Rutter, M. (2000). The Autism Diagnostic Observation Schedule - Generic: A standard measure of social and communication defi cits associated with the spectrum of autism. Journal of Autism and Developmental Disorders, 30, 205-224.
53. Lowery, M. C., Morris, C. A., Ewart, A. K., Brothman, L., Zhu, X. L., Leonard, C. O., Brothman, A. R. (1995). Strong correlation of elastin deletions, detected by FISH, with Williams syndrome: Evaluation of 235 patients. American Journal of Human Genetics, 57, 49-53.
54. Macintosh, K. E., & Dissanayake, C. (2004). The similarities and differences between autistic disorder and Asperger's disorder: A review of the empirical evidence. Journal of Child Psychology and Psychiatry, 45, 421-434.
55. Maj, M. (2005). 'Psychiatric comorbidity': An artefact of current diagnostic systems? British Journal of Psychiatry, 186, 182-184.
56. 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, 576-608.
57. Marshall, C. R., & van der Lely, H. K. J. (2009). Effects of word position and stress on onset cluster production: Evidence from typical development, specifi c language impairment, and dyslexia. Language, 85, 39-57.
58. Mawhood, L., Howlin, P., & Rutter, M. (2000). Autism and developmental receptive language disorder - A comparative follow-up in early adult life: I. Cognitive and language outcomes. Journal of Child Psychology and Psychiatry, 41, 547-559.
59. McGrath, L. M., Pennington, B. F., Shanahan, M. A., Santerre-Lemmon, L. E., Barnard, H. D., Willcutt, E. G., Olson, R. K. (2011). A multiple defi cit model of reading disability and attention-defi cit/hyperactivity disorder: Searching for shared cognitive defi cits. Journal of Child Psychology and Psychiatry, 52, 547-557.
60. Morton, J. (2004). Understanding developmental disorders: A causal modelling approach. Malden, MA: Blackwell.
61. Morton, J., & Frith, U. (1995). Causal modelling: A structural approach to developmental psychopathology. In D. Cicchetti & D. J. Cohen (Eds.), Developmental psychopathology: Vol. 1. Theory and methods (pp. 357-390). New York, NY: Wiley.
62. Neale, M. C., & Kendler, K. S. (1995). Models of comorbidity for multifactorial disorders. American Journal of Human Genetics, 57, 935-953.
63. Paloyelis, Y., Rijsdijk, F., Wood, A. C., Asherson, P., & Kuntsi, J. (2010). The genetic association between ADHD symptoms and reading diffi culties: The role of inattentiveness and IQ. Journal of Abnormal Child Psychology, 38, 1083-1095.
64. Paracchini, S., Scerri, T., & Monaco, A. P., (2007). The genetic lexicon of dyslexia. Annual Review of Genomics and Human Genetics, 8, 57-79.
65. Pennington, B. F. (2006). From single to multiple defi cit models of developmental disorders. Cognition, 101, 385-413.
66. Pennington, B. F., Groisser, D., & Welsh, M. C. (1993). Contrasting cognitive defi cits in attention defi cit hyperactivity disorder versus reading disability. Developmental Psychology, 29, 511-523.
67. Peoples, R., Franke, Y., Wang, Y., Perez-Jurado, L., Paperna, T., Cisco, M., & Francke, U. (2000). A physical map, including a BAC/PAC clone contig, of the Williams- Beuren syndrome deletion region at 7q11.23. American Journal of Human Genetics, 66, 47-68.
68. Rice, M. L., Wexler, K., & Cleave, P. L. (1995). Specifi c language impairment as a period of extended optional infi nitive. Journal of Speech and Hearing Research, 38, 850-863.
69. Rice, M. L., Smith, S. D., & Gayan, J. (2009). Convergent genetic linkage and associations to language, speech, and reading measures in families of probands with specifi c language impairment. Journal of Neurodevelopmental Disorders, 1, 264-282.
70. Riches, N. G., Loucas, T., Baird, G., Charman, T., & Simonoff, E. (2010). Non-word repetition in adolescents with specifi c language impairment and autism plus language impairments: A qualitative analysis. Journal of Communication Disorders, 44, 23-36.
71. Risi, S., Lord, C., Gotham, K., Corsello, C., Chrysler, C., Szatmari, P., Pickles, A. (2006). Combining information from multiple sources in the diagnosis of autism spectrum disorder. Journal of the American Academy of Child and Adolescent Psychiatry, 45, 1094-1103.
72. Ronald, A., Happé, F., Bolton, P., Butcher, L. M., Price, T. S., Wheelwright, S., Plomin, R. (2006). Genetic heterogeneity between the three components of the autism spectrum: A twin study. Journal of the American Academy of Child and Adolescent Psychiatry, 45, 691-699.
73. Rutter, M. (2005). Aetiology of autism: Findings and questions. Journal of Intellectual Disability Research, 49, 231-238.
74. Rutter, M., Bailey, A., Berument, S. K., LeCouteur, A., Lord, C., & Pickles, A. (2003). Social Communication Questionnaire. Los Angeles, CA: Western Psychological Services.
75. Rutter, M., Caspi, A., Fergusson, D., Horwood, L. J., Goodman, R., Maughan, B., Carroll, J. (2004). Sex differences in developmental reading disability: New fi ndings from 4 epidemiological studies. Journal of the American Medical Association, 291, 2007-2012.
76. Service, E. (1992). Phonology, working memory, and foreign-language learning. Quarterly Journal of Experimental Psychology, 45A, 21-50.
77. Shafritz, K. M., Marchione, K. E., Gore, J. C., Shaywitz, S. E., & Shaywitz, B. A. (2004). The effects of methylphenidate on neural systems of attention in attention defi cit hyperactivity disorder. American Journal of Psychiatry, 161, 1990-1997.
78. Simonoff, E., Pickles, A., Charman, T., Chandler, S., Loucas, T., & Baird, G. (2008). Psychiatric disorders in children with autism spectrum disorders: Prevalence, comorbidity, and associated factors in a population-derived sample. Journal of the American Academy of Child and Adolescent Psychiatry, 47, 921-929.
79. SLI Consortium. (2002). A genome-wide scan identifi es two novel loci involved in specifi c language impairment. American Journal of Human Genetics, 70, 384-398.
80. SLI Consortium. (2004). Highly signifi cant linkage to the SLI1 locus in an expanded sample of individuals affected by specifi c language impairment. American Journal of Human Genetics, 74, 1225-1238.
81. Stone, W. L., Lee, E. B., Ashford, L., Brissie, J., Hepburn, S. L., Coonrod, E. E., & Weiss, B. H. (1999). Can autism be diagnosed accurately in children under 3 years? Journal of Child Psychology and Psychiatry, 40, 219-226.
82. Stothard, S. E., Snowling, M. J., Bishop, D. V. M., Chipchase, B. B., & Kaplan, C. A. (1998). Language-impaired preschoolers: A follow-up into adolescence. Journal of Speech Language and Hearing Research, 41, 407-418.
83. Stuss, D. T., & Knight, R. T. (2002). Principles of frontal lobe function. Oxford, UK: Oxford University Press.
84. Tager-Flusberg, H. (2004). Strategies for conducting research on language in autism. Journal of Autism and Developmental Disorders, 34, 75-80.
85. Taylor, E., Schachar, R., Thorley, G., & Wieselberg, M. (1986). Conduct disorder and hyperactivity: I. Separation of hyperactivity and antisocial conduct in British child psychiatric patients. British Journal of Psychiatry, 149, 760-768.
86. Thorell, L. B., & Wåhlstedt, C. (2006). Executive functioning defi cits in relation to symptoms of ADHD and/or ODD in preschool children. Infant and Child Development, 15, 503-518.
87. Tomblin, J. B., Freese, P. R., & Records, N. L. (1992). Diagnosing specifi c language impairment in adults for the purpose of pedigree analysis. Journal of Speech and Hearing Research, 35, 832-843.
88. Tomblin, J. B., Records, N. L., Buckwalter, P., Zhang, X. Y., Smith, E., & O'Brien, M. (1997). Prevalence of specifi c language impairment in kindergarten children. Journal of Speech Language and Hearing Research, 40, 1245-1260.
89. Tomblin, J. B., Hafeman, L. L., & O'Brien, M. (2003). Autism and autism risk in siblings of children with specifi c language impairment. International Journal of Language & Communication Disorders, 38, 235-250.
90. Velez, C. N., Johnson, J., & Cohen, P. (1989). A longitudinal analysis of selected riskfactors for childhood psychopathology. Journal of the American Academy of Child and Adolescent Psychiatry, 28, 861-864.
91. van Praag, H. M. (1996). Comorbidity (psycho) analysed. British Journal of Psychiatry, 168(Suppl. 30), 129-134.
92. van Praag, H. M. (2000). Nosologomania: A disorder of psychiatry. World Journal of Biological Psychiatry, 1, 151-158.
93. Vernes, S. C., Newbury, D. F., Abrahams, B. S, Winchester, L., Nicod, J., Groszer, M., Fisher, S. E. (2008). A functional genetic link between distinct developmental language disorders. New England Journal of Medicine, 359, 2337-2345.
94. Whitehouse, A. J. O., Barry, J. G., & Bishop, D. V. M. (2008). Further defi ning the language impairment of autism: Is there a specifi c language impairment subtype? Journal of Communication Disorders, 41, 319-336.
95. Whitehouse, A. J. O., Bishop, D. V. M., Ang, Q. W., Pennell, C. E., & Fisher, S. E. (2011). CNTNAP2 variants affect early language development in the general population. Genes, Brain, and Behavior, 10, 451-456.
96. Willcutt, E. G., & Pennington, B. F. (2000). Psychiatric comorbidity in children and adolescents with reading disability. Journal of Child Psychology and Psychiatry, 41, 1039-1048.
97. Willcutt, E. G., Pennington, B. F., Boada, R., Ogline, J. S., Tunick, R. A., Chhabildas, N. A., & Olson, R. K. (2001). A comparison of the cognitive defi cits in reading disability and attention-defi cit/hyperactivity disorder. Journal of Abnormal Psychology, 110, 157-172.
98. Willcutt, E. G., Pennington, B. F., Smith, S. D., Cardon, L. R., Gayan, J., Knopik, V. S., DeFries, J. C. (2002). Quantitative trait locus for reading disability on chromosome 6p is pleiotropic for attention-defi cit hyperactivity disorder. American Journal of Medical Genetics, 114, 260-268.
99. Willcutt, E. G., Pennington, B. F., Olson, R. K., & DeFries, J. C. (2007). Understanding comorbidity: A twin study of reading disability and attention-defi cit/hyperactivity disorder. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics, 144B, 709-714.
100. Willcutt, E. G., Sonuga-Barke, E. J. S., Nigg, J. T., & Sergeant, J. A. (2008). Recent developments in neuropsychological models of childhood psychiatric disorders. In Advances in Biological Psychiatry, 24, 195-226.
101. Wilens, T. E., & Spencer, T. J. (2000). The stimulants revisited. Child and Adolescent Psychiatric Clinics of North America, 9, 573-603.
102. Williams, D., Botting, N., & Boucher, J. (2008). Language in autism and specifi c language impairment: Where are the links? Psychological Bulletin, 134, 944-963.
103. Williams, D., Payne, H., & Marshall, C. R. (2012). Non-word repetition impairment in autism and specifi c language impairment: Evidence for distinct underlying neurocognitive causes. In press, Journal of Autism and Developmental Disorders.
104. Wing, L., & Gould, J. (1979). Severe impairments of social-interaction and associated abnormalities in children: Epidemiology and classifi cation. Journal of Autism and Developmental Disorders, 9, 11-29.
105. World Health Organisation (1993). International classifi cation of mental and behavioural disorders: Clinical descriptions and diagnostic guidelines (10th ed.). Geneva, Switzerland: World Health Organisation.