Skip to main content
Log in

Abnormal Corpus Callosum Connectivity, Socio-communicative Deficits, and Motor Deficits in Children with Autism Spectrum Disorder: A Diffusion Tensor Imaging Study

  • Original Paper
  • Published:
Journal of Autism and Developmental Disorders Aims and scope Submit manuscript

Abstract

In addition to social and communicative deficits, many studies have reported motor deficits in autism spectrum disorder (ASD). This study investigated the macro and microstructural properties of the corpus callosum (CC) of 18 children with ASD and 12 typically developing controls using diffusion tensor imaging tractography. We aimed to explore whether abnormalities of the CC were related to motor deficits, as well as social and communication deficits in children with ASD. The ASD group displayed abnormal macro and microstructure of the total CC and its subdivisions and its structural properties were related to socio-communicative deficits, but not to motor deficits in ASD. These findings advance our understanding of the contributions of the CC to ASD symptoms.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

References

  • American Psychiatric Association. (2000). Diagnostic and statistical manual of mental disorders (4th ed. text revision). Washington, DC: American Psychiatric Association.

  • Aoki, Y., Abe, O., Nippashi, Y., & Yamasue, H. (2013). Comparison of white matter integrity between autism spectrum disorder subjects and typically developing individuals: A meta-analysis of diffusion tensor imaging tractography studies. Molecular Autism,. doi:10.1186/2040-2392-4-25.

    PubMed Central  PubMed  Google Scholar 

  • Bakhtiari, R., Zürcher, N. R., Rogier, O., Russo, B., Hippolyte, L., Granziera, C., et al. (2012). Differences in white matter reflect atypical developmental trajectory in autism: A tract-based spatial statistics study. NeuroImage (Amst),. doi:10.1016/j.nicl.2012.09.001.

    Google Scholar 

  • Barnea-Goraly, N., Kwon, H., Menon, V., Eliez, S., Lotspeich, L., & Reiss, A. L. (2004). White matter structure in autism: Preliminary evidence from diffusion tensor imaging. Biological Psychiatry, 55, 323–326.

    Article  PubMed  Google Scholar 

  • Beaule, V., Tremblay, S., & Theoret, H. (2012). Interhemispheric control of unilateral movement. Neural Plasticity,. doi:10.1155/2012/627816.

    PubMed Central  PubMed  Google Scholar 

  • Benjamini, Y., & Hochberg, Y. (1995). Controlling the false discovery rate: A practical and powerful approach to multiple testing. Journal of the Royal Statistical Society. Series B (Methodological), 57, 289–300.

    Google Scholar 

  • Bloom, J. S., & Hynd, G. W. (2005). The role of the corpus callosum in interhemispheric transfer of information: Excitation or inhibition? Neuropsychology Review, 15, 59–71.

    Article  PubMed  Google Scholar 

  • Budde, M. D., Xie, M., Cross, A. H., & Song, S. K. (2009). Axial diffusivity is the primary correlate of axonal injury in the experimental autoimmune encephalomyelitis spinal cord: A quantitative pixelwise analysis. Journal of Neuroscience, 29, 2805–2813.

    Article  PubMed Central  PubMed  Google Scholar 

  • Cardinale, R. C., Shih, P., Fishman, I., Ford, L. M., & Muller, R. A. (2013). Pervasive rightward asymmetry shifts of functional networks in autism spectrum disorder. JAMA Psychiatry,. doi:10.1001/jamapsychiatry.2013.382.

    PubMed  Google Scholar 

  • Casanova, M. F., El-Baz, A., Mott, M., Mannheim, G., Hassan, H., Fahmi, R., et al. (2009). Reduced gyral window and corpus callosum size in autism: Possible macroscopic correlates of a minicolumnopathy. Journal of Autism and Developmental Disorders, 39, 751–764.

    Article  PubMed Central  PubMed  Google Scholar 

  • Cheng, Y., Chou, K. H., Chen, I. Y., Fan, Y. T., Decety, J., & Lin, C. P. (2010). Atypical development of white matter microstructure in adolescents with autism spectrum disorders. Neuroimage, 50, 873–882.

    Article  PubMed  Google Scholar 

  • Clawson, A., Clayson, P. E., South, M., Bigler, E. D., & Larson, M. J. (2013). An electrophysiological investigation of interhemispheric transfer time in children and adolescents with high-functioning autism spectrum disorders. Journal of Autism and Developmental Disorders,. doi:10.1007/s10803-013-1895-7.

    PubMed  Google Scholar 

  • Corbett, B. A., Carmean, V., Ravizza, S., Wendelken, C., Henry, M. L., Carter, C., et al. (2009). A functional and structural study of emotion and face processing in children with autism. Psychiatry Research, 173, 196–205.

    Article  PubMed Central  PubMed  Google Scholar 

  • Courchesne, E., Karns, C. M., Davis, H. R., Ziccardi, R., Carper, R. A., Tigue, Z. D., et al. (2001). Unusual brain growth patterns in early life in patients with autistic disorder: An MRI study. Neurology, 57, 245–254.

    Article  PubMed  Google Scholar 

  • De Fosse, L., Hodge, S. M., Makris, N., Kennedy, D. N., Caviness, V. S, Jr, McGrath, L., et al. (2004). Language-association cortex asymmetry in autism and specific language impairment. Annals of Neurology, 56, 757–766.

    Article  PubMed  Google Scholar 

  • de Laat, K. F., Tuladhar, A. M., van Norden, A. G. W., Norris, D. G., Zwiers, M. P., & de Leeuw, F.-E. (2011). Loss of white matter integrity is associated with gait disorders in cerebral small vessel disease. Brain, 134, 73–83.

    Article  PubMed  Google Scholar 

  • Dennis, M., Francis, D. J., Cirino, P. T., Schachar, R., Barnes, M. A., & Fletcher, J. M. (2009). Why IQ is not a covariate in cognitive studies of neurodevelopmental disorders. Journal of the International Neuropsychological Society, 15, 331–343.

    Article  PubMed Central  PubMed  Google Scholar 

  • Douaud, G., Jbabdi, S., Behrens, T. E., Menke, R. A., Gass, A., Monsch, A. U., et al. (2011). DTI measures in crossing-fibre areas: Increased diffusion anisotropy reveals early white matter alteration in MCI and mild Alzheimer’s disease. Neuroimage, 55, 880–890.

    Article  PubMed  Google Scholar 

  • Eliassen, J. C., Baynes, K., & Gazzaniga, M. S. (2000). Anterior and posterior callosal contributions to simultaneous bimanual movements of the hands and fingers. Brain, 123(Pt 12), 2501–2511.

    Article  PubMed  Google Scholar 

  • Fournier, K. A., Hass, C. J., Naik, S. K., Lodha, N., & Cauraugh, J. H. (2010). Motor coordination in autism spectrum disorders: A synthesis and meta-analysis. Journal of Autism and Developmental Disorders, 40, 1227–1240.

    Article  PubMed  Google Scholar 

  • Frazier, T. W., Keshavan, M. S., Minshew, N. J., & Hardan, A. Y. (2012). A two-year longitudinal MRI study of the corpus callosum in autism. Journal of Autism and Developmental Disorders, 42, 2312–2322.

    Article  PubMed  Google Scholar 

  • Freitag, C. M., Luders, E., Hulst, H. E., Narr, K. L., Thompson, P. M., Toga, A. W., et al. (2009). Total brain volume and corpus callosum size in medication-naive adolescents and young adults with autism spectrum disorder. Biological Psychiatry, 66, 316–319.

    Article  PubMed Central  PubMed  Google Scholar 

  • Gage, N. M., Juranek, J., Filipek, P. A., Osann, K., Flodman, P., Isenberg, A. L., et al. (2009). Rightward hemispheric asymmetries in auditory language cortex in children with autistic disorder: An MRI investigation. Journal of Neurodevelopmental Disorders, 1, 205–214.

    Article  PubMed Central  PubMed  Google Scholar 

  • Glazebrook, C., Gonzalez, D., Hansen, S., & Elliott, D. (2009). The role of vision for online control of manual aiming movements in persons with autism spectrum disorders. Autism, 13, 411–433.

    Article  PubMed  Google Scholar 

  • Hanaie, R., Mohri, I., Kagitani-Shimono, K., Tachibana, M., Azuma, J., Matsuzaki, J., et al. (2013). Altered microstructural connectivity of the superior cerebellar peduncle is related to motor dysfunction in children with autistic spectrum disorders. Cerebellum,. doi:10.1007/s12311-013-0475-x.

    PubMed  Google Scholar 

  • Hardan, A. Y., Libove, R. A., Keshavan, M. S., Melhem, N. M., & Minshew, N. J. (2009a). A preliminary longitudinal magnetic resonance imaging study of brain volume and cortical thickness in autism. Biological Psychiatry, 66, 320–326.

    Article  PubMed Central  PubMed  Google Scholar 

  • Hardan, A. Y., Pabalan, M., Gupta, N., Bansal, R., Melhem, N. M., Fedorov, S., et al. (2009b). Corpus callosum volume in children with autism. Psychiatry Research, 174, 57–61.

    Article  PubMed Central  PubMed  Google Scholar 

  • Haxby, J. V., Hoffman, E. A., & Gobbini, M. I. (2000). The distributed human neural system for face perception. Trends in Cognitive Sciences, 4, 223–233.

    Article  PubMed  Google Scholar 

  • Heim, S., Amunts, K., Hensel, T., Grande, M., Huber, W., Binkofski, F., et al. (2012). The role of human parietal area 7A as a link between sequencing in hand actions and in overt speech production. Frontiers in Psychology,. doi:10.3389/fpsyg.2012.00534.

    Google Scholar 

  • Henderson, S., Sugden, D., & Barnett, A. L. (2007). The movement assessment battery for children (2nd ed.). London: The Psychological Corporation.

    Google Scholar 

  • Herbert, M. R., Harris, G. J., Adrien, K. T., Ziegler, D. A., Makris, N., Kennedy, D. N., et al. (2002). Abnormal asymmetry in language association cortex in autism. Annals of Neurology, 52, 588–596.

    Article  PubMed  Google Scholar 

  • Hofer, S., & Frahm, J. (2006). Topography of the human corpus callosum revisited—comprehensive fiber tractography using diffusion tensor magnetic resonance imaging. Neuroimage, 32, 989–994.

    Article  PubMed  Google Scholar 

  • Huang, H., Zhang, J., Jiang, H., Wakana, S., Poetscher, L., Miller, M. I., et al. (2005). DTI tractography based parcellation of white matter: Application to the mid-sagittal morphology of corpus callosum. Neuroimage, 26, 195–205.

    Article  PubMed  Google Scholar 

  • Huang, H., Zhang, J., van Zijl, P. C., & Mori, S. (2004). Analysis of noise effects on DTI-based tractography using the brute-force and multi-ROI approach. Magnetic Resonance in Medicine, 52, 559–565.

    Article  PubMed  Google Scholar 

  • Innocenti, G. M. (2009). Dynamic interactions between the cerebral hemispheres. Experimental Brain Research, 192, 417–423.

    Article  PubMed  Google Scholar 

  • Jansiewicz, E. M., Goldberg, M. C., Newschaffer, C. J., Denckla, M. B., Landa, R., & Mostofsky, S. H. (2006). Motor signs distinguish children with high functioning autism and Asperger’s syndrome from controls. Journal of Autism and Developmental Disorders, 36, 613–621.

    Article  PubMed  Google Scholar 

  • Jasmin, E., Couture, M., McKinley, P., Reid, G., Fombonne, E., & Gisel, E. (2009). Sensori-motor and daily living skills of preschool children with autism spectrum disorders. Journal of Autism and Developmental Disorders, 39, 231–241.

    Article  PubMed  Google Scholar 

  • Johnson, B. P., Rinehart, N. J., Papadopoulos, N., Tonge, B., Millist, L., White, O., et al. (2012). A closer look at visually guided saccades in autism and Asperger’s disorder. Frontiers in Integrative Neuroscience,. doi:10.3389/fnint.2012.00099.

    Google Scholar 

  • Jones, D. K., Knosche, T. R., & Turner, R. (2013). White matter integrity, fiber count, and other fallacies: The do’s and don’ts of diffusion MRI. Neuroimage, 73, 239–254.

    Article  PubMed  Google Scholar 

  • Kana, R. K., Libero, L. E., Hu, C. P., Deshpande, H. D., & Colburn, J. S. (2012). Functional brain networks and white matter underlying theory-of-mind in autism. Social Cognitive and Affective Neuroscience,. doi:10.1093/scan/nss106.

    PubMed Central  Google Scholar 

  • Keary, C. J., Minshew, N. J., Bansal, R., Goradia, D., Fedorov, S., Keshavan, M. S., et al. (2009). Corpus callosum volume and neurocognition in autism. Journal of Autism and Developmental Disorders, 39, 834–841.

    Article  PubMed Central  PubMed  Google Scholar 

  • 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.

    Article  PubMed Central  PubMed  Google Scholar 

  • Knaus, T. A., Silver, A. M., Dominick, K. C., Schuring, M. D., Shaffer, N., Lindgren, K. A., et al. (2009). Age-related changes in the anatomy of language regions in autism spectrum disorder. Brain Imaging and Behavior, 3, 51–63.

    Article  PubMed Central  PubMed  Google Scholar 

  • Kumar, A., Sundaram, S. K., Sivaswamy, L., Behen, M. E., Makki, M. I., Ager, J., et al. (2010). Alterations in frontal lobe tracts and corpus callosum in young children with autism spectrum disorder. Cerebral Cortex, 20, 2103–2113.

    Article  PubMed  Google Scholar 

  • Lau, Y. C., Hinkley, L. B., Bukshpun, P., Strominger, Z. A., Wakahiro, M. L., Baron-Cohen, S., et al. (2013). Autism traits in individuals with agenesis of the corpus callosum. Journal of Autism and Developmental Disorders, 43, 1106–1118.

    Article  PubMed Central  PubMed  Google Scholar 

  • Leary, M. R., & Hill, D. A. (1996). Moving on: Autism and movement disturbance. Mental Retardation, 34, 39–53.

    PubMed  Google Scholar 

  • Lebel, C., Benner, T., & Beaulieu, C. (2012). Six is enough? Comparison of diffusion parameters measured using six or more diffusion-encoding gradient directions with deterministic tractography. Magnetic Resonance in Medicine, 68, 474–483.

    Article  PubMed  Google Scholar 

  • Lebel, C., Caverhill-Godkewitsch, S., & Beaulieu, C. (2010). Age-related regional variations of the corpus callosum identified by diffusion tensor tractography. Neuroimage, 52, 20–31.

    Article  PubMed  Google Scholar 

  • Lord, C., Risi, S., Lambrecht, L., Cook, E. H, Jr, Leventhal, B. L., DiLavore, P. C., et al. (2000). The autism diagnostic observation schedule-generic: A standard measure of social and communication deficits associated with the spectrum of autism. Journal of Autism and Developmental Disorders, 30, 205–223.

    Article  PubMed  Google Scholar 

  • Minshew, N. J., Sung, K., Jones, B. L., & Furman, J. M. (2004). Underdevelopment of the postural control system in autism. Neurology, 63, 2056–2061.

    Article  PubMed  Google Scholar 

  • Minshew, N. J., & Williams, D. L. (2007). The new neurobiology of autism: Cortex, connectivity, and neuronal organization. Archives of Neurology, 64, 945–950.

    Article  PubMed Central  PubMed  Google Scholar 

  • Moes, P., Schilmoeller, K., & Schilmoeller, G. (2009). Physical, motor, sensory and developmental features associated with agenesis of the corpus callosum. Child: Care, Health and Development, 35, 656–672.

    Google Scholar 

  • Mori, S., Crain, B. J., Chacko, V. P., & van Zijl, P. C. (1999). Three-dimensional tracking of axonal projections in the brain by magnetic resonance imaging. Annals of Neurology, 45, 265–269.

    Article  PubMed  Google Scholar 

  • Mostofsky, S. H., & Ewen, J. B. (2011). Altered connectivity and action model formation in autism is autism. Neuroscientist, 17, 437–448.

    Article  PubMed Central  PubMed  Google Scholar 

  • Mostofsky, S. H., Powell, S. K., Simmonds, D. J., Goldberg, M. C., Caffo, B., & Pekar, J. J. (2009). Decreased connectivity and cerebellar activity in autism during motor task performance. Brain, 132, 2413–2425.

    Article  PubMed Central  PubMed  Google Scholar 

  • Noriuchi, M., Kikuchi, Y., Yoshiura, T., Kira, R., Shigeto, H., Hara, T., et al. (2010). Altered white matter fractional anisotropy and social impairment in children with autism spectrum disorder. Brain Research, 1362, 141–149.

    Article  PubMed  Google Scholar 

  • Oldfield, R. C. (1971). The assessment and analysis of handedness: The Edinburgh inventory. Neuropsychologia, 9, 97–113.

    Article  PubMed  Google Scholar 

  • Pannek, K., Mathias, J. L., Bigler, E. D., Brown, G., Taylor, J. D., & Rose, S. (2010). An automated strategy for the delineation and parcellation of commissural pathways suitable for clinical populations utilising high angular resolution diffusion imaging tractography. Neuroimage, 50, 1044–1053.

    Article  PubMed  Google Scholar 

  • Park, H. J., Kim, J. J., Lee, S. K., Seok, J. H., Chun, J., Kim, D. I., et al. (2008). Corpus callosal connection mapping using cortical gray matter parcellation and DT-MRI. Human Brain Mapping, 29, 503–516.

    Article  PubMed  Google Scholar 

  • Paus, T., & Toro, R. (2009). Could sex differences in white matter be explained by g ratio? Frontiers in Neuroanatomy,. doi:10.3389/neuro.05.014.2009.

    PubMed Central  PubMed  Google Scholar 

  • Prigge, M. B., Lange, N., Bigler, E. D., Merkley, T. L., Neeley, E. S., Abildskov, T. J., et al. (2013). Corpus callosum area in children and adults with autism. Research in Autism Spectrum Disorders, 7, 221–234.

    Article  PubMed Central  PubMed  Google Scholar 

  • Qiu, A., Adler, M., Crocetti, D., Miller, M. I., & Mostofsky, S. H. (2010). Basal ganglia shapes predict social, communication, and motor dysfunctions in boys with autism spectrum disorder. Journal of the American Academy of Child and Adolescent Psychiatry, 49, 539–551.

    PubMed  Google Scholar 

  • Rademaker, K. J., Lam, J. N., Van Haastert, I. C., Uiterwaal, C. S., Lieftink, A. F., Groenendaal, F., et al. (2004). Larger corpus callosum size with better motor performance in prematurely born children. Seminars in Perinatology, 28, 279–287.

    Article  PubMed  Google Scholar 

  • Redcay, E. (2008). The superior temporal sulcus performs a common function for social and speech perception: Implications for the emergence of autism. Neuroscience and Biobehavioral Reviews, 32, 123–142.

    Article  PubMed  Google Scholar 

  • Rinehart, N. J., Tonge, B. J., Bradshaw, J. L., Iansek, R., Enticott, P. G., & McGinley, J. (2006). Gait function in high-functioning autism and Asperger’s disorder: Evidence for basal-ganglia and cerebellar involvement? European Child and Adolescent Psychiatry, 15, 256–264.

    Article  PubMed  Google Scholar 

  • Schwartz, E. D., Cooper, E. T., Fan, Y., Jawad, A. F., Chin, C. L., Nissanov, J., et al. (2005). MRI diffusion coefficients in spinal cord correlate with axon morphometry. NeuroReport, 16, 73–76.

    Article  PubMed  Google Scholar 

  • Shukla, D. K., Keehn, B., Lincoln, A. J., & Muller, R. A. (2010). White matter compromise of callosal and subcortical fiber tracts in children with autism spectrum disorder: A diffusion tensor imaging study. Journal of the American Academy of Child and Adolescent Psychiatry, 49, 1269–1278., 1278 e1261–e1262.

    PubMed Central  PubMed  Google Scholar 

  • Song, S. K., Sun, S. W., Ju, W. K., Lin, S. J., Cross, A. H., & Neufeld, A. H. (2003). Diffusion tensor imaging detects and differentiates axon and myelin degeneration in mouse optic nerve after retinal ischemia. Neuroimage, 20, 1714–1722.

    Article  PubMed  Google Scholar 

  • Thomas, C., Humphreys, K., Jung, K. J., Minshew, N., & Behrmann, M. (2011). The anatomy of the callosal and visual-association pathways in high-functioning autism: A DTI tractography study. Cortex, 47, 863–873.

    Article  PubMed Central  PubMed  Google Scholar 

  • Tournier, J. D., Mori, S., & Leemans, A. (2011). Diffusion tensor imaging and beyond. Magnetic Resonance in Medicine, 65, 1532–1556.

    Article  PubMed Central  PubMed  Google Scholar 

  • Townsend, J., Courchesne, E., & Egaas, B. (1996). Slowed orienting of covert visual-spatial attention in autism: Specific deficits associated with cerebellar and parietal abnormality. Development and Psychopathology, 8, 563–584.

    Article  Google Scholar 

  • Travers, B. G., Adluru, N., Ennis, C., Tromp do, P. M., Destiche, D., Doran, S., et al. (2012). Diffusion tensor imaging in autism spectrum disorder: A review. Autism Research, 5, 289–313.

    Article  PubMed Central  PubMed  Google Scholar 

  • Vidal, C. N., Nicolson, R., DeVito, T. J., Hayashi, K. M., Geaga, J. A., Drost, D. J., et al. (2006). Mapping corpus callosum deficits in autism: An index of aberrant cortical connectivity. Biological Psychiatry, 60, 218–225.

    Article  PubMed  Google Scholar 

  • Vigneau, M., Beaucousin, V., Herve, P. Y., Duffau, H., Crivello, F., Houde, O., et al. (2006). Meta-analyzing left hemisphere language areas: Phonology, semantics, and sentence processing. Neuroimage, 30, 1414–1432.

    Article  PubMed  Google Scholar 

  • Vollm, B. A., Taylor, A. N., Richardson, P., Corcoran, R., Stirling, J., McKie, S., et al. (2006). Neuronal correlates of theory of mind and empathy: A functional magnetic resonance imaging study in a nonverbal task. Neuroimage, 29, 90–98.

    Article  PubMed  Google Scholar 

  • Waiter, G. D., Williams, J. H., Murray, A. D., Gilchrist, A., Perrett, D. I., & Whiten, A. (2005). Structural white matter deficits in high-functioning individuals with autistic spectrum disorder: A voxel-based investigation. Neuroimage, 24, 455–461.

    Article  PubMed  Google Scholar 

  • Wakana, S., Caprihan, A., Panzenboeck, M. M., Fallon, J. H., Perry, M., Gollub, R. L., et al. (2007). Reproducibility of quantitative tractography methods applied to cerebral white matter. Neuroimage, 36, 630–644.

    Article  PubMed Central  PubMed  Google Scholar 

  • Whyatt, C. P., & Craig, C. M. (2012). Motor skills in children aged 7–10 years, diagnosed with autism spectrum disorder. Journal of Autism and Developmental Disorders, 42, 1799–1809.

    Article  PubMed  Google Scholar 

  • Williams, D. L., Cherkassky, V. L., Mason, R. A., Keller, T. A., Minshew, N. J., & Just, M. A. (2013). Brain function differences in language processing in children and adults with autism. Autism Research,. doi:10.1002/aur.1291.

    Google Scholar 

  • Wolff, J. J., Gu, H., Gerig, G., Elison, J. T., Styner, M., Gouttard, S., et al. (2012). Differences in white matter fiber tract development present from 6 to 24 months in infants with autism. American Journal of Psychiatry, 169, 589–600.

    Article  PubMed Central  PubMed  Google Scholar 

  • Wu, Q., Butzkueven, H., Gresle, M., Kirchhoff, F., Friedhuber, A., Yang, Q., et al. (2007). MR diffusion changes correlate with ultra-structurally defined axonal degeneration in murine optic nerve. Neuroimage, 37, 1138–1147.

    Article  PubMed  Google Scholar 

  • Yendiki, A., Koldewyn, K., Kakunoori, S., Kanwisher, N., & Fischl, B. (2013). Spurious group differences due to head motion in a diffusion MRI study. Neuroimage, 88C, 79–90.

    PubMed  Google Scholar 

  • Zwarts, M. J., & Guechev, A. (1995). The relation between conduction velocity and axonal length. Muscle and Nerve, 18, 1244–1249.

    Article  PubMed  Google Scholar 

Download references

Acknowledgments

This work was supported in part by research grants from the Ministry of Education, Culture, Sports, Science and Technology of Japan (23591494 to K.K-S, 24659497 to M.T) and by the Osaka University Program for the Support of Networking among Present and Future Women Researchers (to M.I). We thank Mayumi Wada and Shun Ochi for helping with our volumetric analysis and are grateful to all of the children and parents who participated in this study.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Masako Taniike.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Hanaie, R., Mohri, I., Kagitani-Shimono, K. et al. Abnormal Corpus Callosum Connectivity, Socio-communicative Deficits, and Motor Deficits in Children with Autism Spectrum Disorder: A Diffusion Tensor Imaging Study. J Autism Dev Disord 44, 2209–2220 (2014). https://doi.org/10.1007/s10803-014-2096-8

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10803-014-2096-8

Keywords

Navigation