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Research Article

Deficits in sequential processing manifest in motor and linguistic tasks in a multigenerational family with childhood apraxia of speech

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Pages 163-191 | Received 17 Sep 2012, Accepted 28 Sep 2012, Published online: 22 Jan 2013

References

  • Boersma, P. (2001). Praat, a system for doing phonetics by computer. Glot International, 5(9/10), 341–345.
  • Button, L. A., Peter, B., Stoel-Gammon, C., & Raskind, W. H. (submitted). Associations among measures of sequential processing in motor and linguistics tasks in adults with and without a history of childhood apraxia of speech.
  • Catts, H. W. (1986). Speech production/phonological deficits in reading-disordered children. [Research Support, Non-U.S. Gov't]. Journal of Learning Disabilities, 19(8), 504–508.
  • Cohen, J. (1992). A power primer. Psychological Bulletin, 112(1), 155–159.
  • Desmond, J. E., Gabrieli, J. D., Wagner, A. D., Ginier, B. L., & Glover, G. H. (1997). Lobular patterns of cerebellar activation in verbal working-memory and finger-tapping tasks as revealed by functional MRI. [Research Support, Non-U.S. Gov'tResearch Support, U.S. Gov't, P.H.S.]. Journal of Neuroscience, 17(24), 9675–9685.
  • Dollaghan, C., & Campbell, T. F. (1998). Nonword repetition and child language impairment. [Research Support, U.S. Gov't, P.H.S.]. Journal of Speech Language and Hearing Research, 41(5), 1136–1146.
  • Elsas, L. J.,2nd, Langley, S., Paulk, E. M., Hjelm, L. N., & Dembure, P. P. (1995). A molecular approach to galactosemia. [Research Support, U.S. Gov't, P.H.S.]. European Journal of Pediatrics, 154(7 Suppl 2), S21–S27.
  • Fisher, S. E., Vargha-Khadem, F., Watkins, K. E., Monaco, A. P., & Pembrey, M. E. (1998). Localisation of a gene implicated in a severe speech and language disorder. Nature Genetics, 18(2), 168–170. doi: 10.1038/ng0298-168.
  • Fletcher, S. G. (1972). Time-by-count measurement of diadochokinetic syllable rate. Journal of Speech and Hearing Research, 15(4), 763–770.
  • Goldman, R. F. M. (2000). Goldman-Fristoe Test of Articulation 2. Circle Pines: American Guidance Service.
  • Grasby, P. M., Frith, C. D., Friston, K. J., Bench, C., Frackowiak, R. S., & Dolan, R. J. (1993). Functional mapping of brain areas implicated in auditory-verbal memory function. Brain, 116(Pt 1), 1–20.
  • Gray, R. M., Livingston, R. B., Marshall, R. M., & Haak, R. A. (2000). Reference group data for the Reitan-Indiana Neuropsychological Test Battery for Young Children. Perceptual and Motor Skills, 91(2), 675–682.
  • Gualtieri, C. T., & Johnson, L. G. (2006). Reliability and validity of a computerized neurocognitive test battery, CNS Vital Signs. Archives of Clinical Neuropsychology, 21(7), 623–643. doi: S0887-6177(06)00083-7[pii]10.1016/j.acn.2006.05.007.
  • Khan, L., & Lewis, N. (2002). Khan-Lewis Phonological Analysis, Second Edition. Circle Pines: American Guidance Service.
  • Klapp, S. T. (1995). Motor response programming during simple and choice-reaction time – The role of practice. Journal of Experimental Psychology-Human Perception and Performance, 21(5), 1015–1027.
  • Klapp, S. T. (2003). Reaction time analysis of two types of motor preparation for speech articulation: action as a sequence of chunks [Research Support, Non-U.S. Gov't]. Journal of Motor Behavior, 35(2), 135–150. doi: 10.1080/00222890309602129.
  • Konig, I. R., Schumacher, J., Hoffmann, P., Kleensang, A., Ludwig, K. U., Grimm, T., … Schulte-Korne, G. (2011). Mapping for dyslexia and related cognitive trait loci provides strong evidence for further risk genes on chromosome 6p21. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics, 156B(1), 36–43. doi: 10.1002/ajmg.b.31135.
  • Laffin, J. J., Raca, G., Jackson, C. A., Strand, E. A., Jakielski, K. J., & Shriberg, L. D. (2012). Novel candidate genes and regions for childhood apraxia of speech identified by array comparative genomic hybridization. Genetics in Medicine. doi: 10.1038/gim.2012.72. [Epubs ahead of print]
  • Lai, C. S., Fisher, S. E., Hurst, J. A., Vargha-Khadem, F., & Monaco, A. P. (2001). A forkhead-domain gene is mutated in a severe speech and language disorder. Nature, 413(6855), 519–523. doi: 10.1038/350970735097076 [pii].
  • Leggio, M. G., Tedesco, A. M., Chiricozzi, F. R., Clausi, S., Orsini, A., & Molinari, M. (2008). Cognitive sequencing impairment in patients with focal or atrophic cerebellar damage [Research Support, Non-U.S. Gov't]. Brain, 131(Pt 5), 1332–1343. doi: 10.1093/brain/awn040.
  • Lewis, B. A., Freebairn, L. A., Hansen, A., Gerry Taylor, H., Iyengar, S., & Shriberg, L. D. (2004). Family pedigrees of children with suspected childhood apraxia of speech. Journal of Communication Disorders, 37(2), 157–175. doi: 10.1016/j.jcomdis.2003.08.003S0021992403000765 [pii].
  • Maas, E., Robin, D. A., Wright, D. L., & Ballard, K. J. (2008). Motor programming in apraxia of speech. Brain and Language, 106(2), 107–118. doi: Doi 10.1016/J.Bandl.2008.03.004.
  • MacDermot, K. D., Bonora, E., Sykes, N., Coupe, A. M., Lai, C. S., Vernes, S. C., … Fisher, S. E. (2005). Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits. American Journal of Human Genetics, 76(6), 1074–1080. doi: S0002-9297(07)62902-4 [pii10.1086/430841].
  • Marquardt, T. P., Jacks, A., & Davis, B. L. (2004). Token-to-token variability in developmental apraxia of speech: three longitudinal case studies [Case Reports]. Clinical Linguistics and Phonetics, 18(2), 127–144.
  • McNeil, M. R. (1997). Clinical management of sensorimotor speech disorders. New York: Thieme.
  • McNeil, M. R. (2009). Clinical management of sensorimotor speech disorders (2nd ed.). New York: Thieme.
  • Neau, J. P., Arroyo-Anllo, E., Bonnaud, V., Ingrand, P., & Gil, R. (2000). Neuropsychological disturbances in cerebellar infarcts. Acta Neurologica Scandinavica, 102(6), 363–370.
  • Newbury, D. F., Mari, F., Akha, E. S., Macdermot, K. D., Canitano, R., Monaco, A. P., … Knight, S. J. (2012). Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder. European Journal of Human Genetics. doi: 10.1038/ejhg.2012.166. [Epubs ahead of print]
  • Newmeyer, A. J., Aylward, C., Akers, R., Ishikawa, K., Grether, S., deGrauw, T., … White, J. (2009). Results of the Sensory Profile in children with suspected childhood apraxia of speech [Comparative StudyResearch Support, Non-U.S. Gov't]. Physical & Occupational Therapy in Pediatrics, 29(2), 203–218. doi: 10.1080/01942630902805202.
  • Oldfield, R. C. (1971). The assessment and analysis of handedness: The Edinburgh inventory. Neuropsychologia, 9(1), 97–113.
  • Peter, B., Matsushita, M., & Raskind, W. H. (2012). Motor sequencing deficit as an endophenotype of speech sound disorder: A genome-wide linkage analysis in a multigenerational family. Psychiatric Genetics, 22(5), 226–234. doi: 10.1097/YPG.0b013e328353ae92.
  • Peter, B., & Raskind, W. H. (2011). A multigenerational family study of oral and hand motor sequencing ability provides evidence for a familial speech sound disorder subtype. Top Lang Disord, 31(2), 145–167. doi: 10.1097/TLD.0b013e318217b855.
  • Petersen, S. E., & Fiez, J. A. (1993). The processing of single words studied with positron emission tomography [Research Support, Non-U.S. Gov'Research Support, U.S. Gov't, Non-P.H.S.Research Support, U.S. Gov't, P.H.S.Review]. Annual Review of Neuroscience, 16, 509–530. doi: 10.1146/annurev.ne.16.030193.002453.
  • Raca, G., Baas, B. S., Kirmani, S., Laffin, J. J., Jackson, C. A., Strand, E. A., … Shriberg, L. D. (2012). Childhood apraxia of speech (CAS) in two patients with 16p11.2 microdeletion syndrome. European Journal of Human Genetics. doi: 10.1038/ejhg.2012.165. [Epubs ahead of print]
  • Reynolds, C. R., & Kamphaus, R. W. (2003). RIAS, Reynolds Intellectual Assessment Scales. Lutz, FL: Psychological Assessment Resources.
  • Robbins, J., & Klee, T. (1987). Clinical assessment of oropharyngeal motor development in young children. Journal of Speech and Hearing Disorders, 52(3), 271–277.
  • Shriberg, L. D., Lohmeier, H. L., Campbell, T. F., Dollaghan, C. A., Green, J. R., & Moore, C. A. (2009). A nonword repetition task for speakers with misarticulations: the Syllable Repetition Task (SRT) [Research Support, N.I.H., ExtramuralValidation Studies]. Journal of Speech Language and Hearing Research, 52(5), 1189–1212. doi: 10.1044/1092-4388(2009/08-0047).
  • Shriberg, L. D., Lohmeier, H. L., Strand, E. A., & Jakielski, K. J. (2012). Encoding, memory, and transcoding deficits in Childhood Apraxia of Speech [Research Support, N.I.H., Extramural]. Clinical Linguistics and Phonetics, 26(5), 445–482. doi: 10.3109/02699206.2012.655841. [Epubs ahead of print]
  • Shriberg, L. D., Potter, N. L., & Strand, E. A. (2010). Prevalence and phenotype of childhood apraxia of speech in youth with galactosemia. Journal of Speech Language and Hearing Research. doi: 1092-4388_2010_10-0068 [pii]10.1044/1092-4388(2010/10-0068).
  • Shriberg, L. D., Potter, N. L., & Strand, E. A. (2011). Prevalence and phenotype of childhood apraxia of speech in youth with galactosemia [Research Support, N.I.H., Extramural]. Journal of Speech Language and Hearing Research, 54(2), 487–519. doi: 10.1044/1092-4388(2010/10-0068).
  • Wagner, R. K., Torgesen, J. K., & Rashotte, C. A. (1999). CTOPP, Comprehensive Test of Phonological Processing. Austin, TX: PRO-ED.
  • Wechsler, D. (2002). Wechsler Individual Achievement Test (2nd ed.). New York: Psychological Corporation.
  • Wolf, M. (1986). Rapid alternating stimulus naming in the developmental dyslexias [Research Support, Non-U.S. Gov't Review]. Brain and Language, 27(2), 360–379.
  • Wolf, M., & Denckla, M. (2005). Rapid automatized naming and rapid alternating stimulus tests. Austin: Pro-Ed.
  • Woodcock, R. W. (1998). Woodcock Reading Mastery Tests – Revised. Minneapolis: Pearson.
  • Wright, D. L., Robin, D. A., Rhee, J., Vaculin, A., Jacks, A., Guenther, F. H., & Fox, P. T. (2009). Using the self-select paradigm to delineate the nature of speech motor programming [Research Support, N.I.H., Extramural]. Journal of Speech Language and Hearing Research, 52(3), 755–765. doi: 10.1044/1092-4388(2009/07-0256).

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