79
Views
2
CrossRef citations to date
0
Altmetric
Research Report

Language skills in 5–8‐year‐old children with 22q11 deletion syndrome

, , , , &
Pages 313-333 | Received 17 Feb 2004, Accepted 01 Aug 2005, Published online: 03 Jul 2009

References

  • Bishop D. V. M. Test for Reception of Grammar. University of Manchester, Manchester 1989
  • Bishop D. V. M. Uncommon Understanding. Development and Disorders of Language Comprehension in Children. Psychology Press, Hove 1997
  • Bishop D. V. M., Edmundson A. Language‐impaired 4‐year‐olds: distinguishing transient from persistent impairment. Journal of Speech and Hearing Disorders 1987; 52: 156–173
  • Bjar L. Orden tar form — om barns uttalsutveckling. Barn utvecklar sitt språk, C Liberg, L Bjar. Studentlitteratur, Lund 2003; 103–126
  • Botting N. Narrative as a tool for the assessment of linguistic and pragmatic impairments. Child Language Teaching and Therapy 2002; 18: 1–21
  • Conti‐Ramsden G., Botting N., Simkin Z., Knox E. Follow‐up of children attending infant language units: outcomes at 11 years of age. International Journal of Language and Communication Disorders 2001; 36: 207–219
  • D'Antonio L. L., Scherer N. J., Miller L. L., Kalbfleisch J. H., Bartley J. A. Analysis of speech characteristics in children with velocardiofacial syndrome (VCFS) and children with phenotypic overlap without VCFS. Cleft Palate‐Craniofacial Journal 2001; 39: 455–467
  • Devriendt K., Fryns J. ‐P., Mortier G. The annual incidence of DiGeorge/velocardiofacial syndrome. Journal of Medical Genetics 1998; 35: 789–790
  • Driscoll D. A., Spinner N. B., Budarf M. L., McDonald‐McGinn D. M., Zackai E. H., Goldberg R. B., Shprintzen R. J., Saal H. M., Zonana J., Jones M. C., Mascarello J. T., Emanuel B. S. Deletions and microdeletions of 22q11. 2 in velo‐cardio‐facial syndrome. American Journal of Medical Genetics 1992; 44: 261–268
  • Duffy J. R. Motor Speech Disorders. Substrates, Differential Diagnosis, and Management. Mosby, St Louis, MO 1995
  • Dunn L. M., Dunn L. M. Peabody Picture Vocabulary Test — Revised. American Guidance Service, Circle Pines, MN 1981
  • Espinosa Å., Lundgren M. Normalspråkiga 3.5‐åringars aktiva och passiva ordförråd. 1997, Master's thesis, Karolinska Institutet, Stockholm
  • Gerdes M., Solot C., Wang P. P., Moss E., Larossa D., Randall P., Goldmuntz E., Clark B. J., Driscoll D. A., Jawad A., Emanuel B. S., McDonald‐McGinn D. M., Batshaw M. L., Zackai E. H. Cognitive and behavior profile of preschool children with chromosome 22q11. 2 deletion. American Journal of Medical Genetics 1999; 85: 127–133
  • Glaser B., Mumme D. L., Blasey C., Morris M. A., Dahoun S. P., Antonarakis S. E., Reiss A. L., Eliez S. Language skills in children with velocardiofacial syndrome (deletion 22q11. 2). Journal of Pediatrics 2002; 140: 753–758
  • Goldberg R., Motzkin B., Marion R., Scambler P. J., Shprintzen R. J. Velo‐Cardio‐Facial Syndrome: a review of 120 Patients. American Journal of Medical Genetics 1993; 45: 313–319
  • Golding‐Kushner K. J., Weller G., Shprintzen R. J. Velo‐cardio‐facial syndrome: language and psychological profiles. Journal of Craniofacial Genetics and Developmental Biology 1985; 5: 259–266
  • Grunwell P. Clinical Phonology. Croom Helm, Beckenham 1982
  • Haapanen M. ‐L., Somer M. Velocardiofacial syndrome: analysis of phoniatric and other clinical findings. Folia Phoniatrica 1993; 43: 239–246
  • Hellquist B. Swedish Version. Metafon på svenska. Pedagogisk Design, Skivarp 1992
  • Holmberg E., Lundälv E. Swedish Version. TROG — Svensk Manual. SIH läromedel, Gothenburg 1989
  • ISO 389. Reference Zero for the Calibration of Audiometric Equipment. 1994–98, (ISO)
  • ISO 8253‐1. Audiometric Test Methods. Part I. Basic Pure Tone Air and Bone Conduction Threshold Audiometry. 1989, (ISO)
  • Lewis B. A., Freebairn L., Heeger S., Cassidy S. B. Speech and language skills in individuals with Prader–Willi syndrome. American Journal of Speech–Language Pathology 2002; 11: 285–294
  • Lipson A. H., Yuille D., Angel M., Thomson P. G., Vandervoord J. G., Beckenham E. J. Velocardiofacial (Shprintzen) syndrome: an important syndrome for the dysmorphologist to recognise. Journal of Medical Genetics 1991; 28: 596–604
  • Magnusson E. The phonology of language disordered children. Production, perception, and awareness. 1983, Doctoral thesis, Lund University, Lund
  • McDonald‐McGinn D. M., Larossa D., Goldmuntz E., Sullivan K., Eicher P., Gerdes M., Moss E., Wang P., Solot C., Schultz P., Lynch D., Bingham P., Keenan G., Weinzimer S., Ming J. E., Driscoll D., Clark Iii B. J., Markowitz R., Cohen A., Moshang T., Pasquariello P., Randall P., Emanuel B. S., Zackai E. H. The 22q11. 2 deletion: screening, diagnostic workup, and outcome of results; report on 181 patients. Genetic Testing 1997; 1: 99–108
  • Merritt D. D., Liles B. Z. Narrative analysis: clinical applications of story generation and story retelling. Journal of Speech and Hearing Disorders 1989; 54: 438–447
  • Moss E. M., Batshaw M. L., Solot C. B., Gerdes M., McDonald‐McGinn D. M., Driscoll D. A., Emanuel B. S., Zackai E. H., Wang P. P. Psychoeducational profile of the 22q11. 2 microdeletion: a complex pattern. Journal of Pediatrics 1999; 134: 193–198
  • Nayak J., Sell D. Velocardiofacial syndrome. Bulletin Royal college of SL Therapists. 1998, March
  • Niklasson L., Rasmussen P., Óskarsdóttir S., Gillberg C. Neuropsychiatric disorders in the 22q11 deletion syndrome. Genetics in Medicine 2001; 3: 79–84
  • Niklasson L., Rasmussen P., Óskarsdóttir S., Gillberg C. Chromosome 22q11 deletion syndrome (CATCH22): neuropsychiatric and neuropsychological aspects. Developmental Medicine and Child Neurology 2002; 44: 44–50
  • Óskarsdóttir S., Vujic M., Fast A. Incidence and prevalence of the 22q11 deletion syndrome; a population based study in western Sweden. Archives of Diseases in Childhood 2004; 89: 148–151
  • Paul R., Smith R. L. Narrative skills in 4‐year‐olds with normal, impaired, and late‐developing language. Journal of Speech and Hearing Research 1993; 36: 592–598
  • Persson C., Lohmander A., Jönsson R., Óskarsdóttir S., Söderpalm E. A prospective cross‐sectional study of speech in patients with the 22q11 deletion syndrome. Journal of Communication Disorders 2003; 36: 13–47
  • Renfrew C. The Renfrew Language Scales: Bus Story Test — A Test of Narrative Speech. Winslow, Bicester 1997
  • Reuterskiöld‐Wagner C., Sahlén B., Nettelbladt U. What's the story? Narration and comprehension in Swedish preschool children with language impairment. Child Language Teaching and Therapy 1999; 15: 113–137
  • Rommel N., Van Trappen G., Swillen A., Devriendt K., Feenstra L., Fryns J. P. Retrospective analysis of feeding and speech disorders in 50 patients with velo‐cardio‐facial syndrome. Genetic Counseling 1999; 10: 71–78
  • Ryan A. K., Goodship J. A., Wilson D. I., Philip N., Levy A., Seidel H., Schuffenhauer S., Oechsler H., Belohradsky B., Prieur M., Aurias A., Raymond F. I., Clayton‐Smith J., Hatchwell E., McKeown C., Beemer F. A., Dallapiccola B., Novelli G., Hurst J. A., Ignatius J., Green A. J., Winter R. M., Brueton L., Brondum‐Nielsen K., Stewart F., Van Essen T., Patton M., Paterson J., Scambler P. J. Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study. Journal of Medical Genetics 1997; 34: 798–804
  • Scherer N. J., D'Antonio L. L., Kalbfleisch J. H. Early speech and language development in children with velocardiofacial syndrome. American Journal of Medical Genetics (Neuropsychiatric Genetics) 1999; 88: 714–723
  • Scherer N. J., D'Antonio L. L., Rodgers J. R. Profiles of communication disorder in children with velocardiofacial syndrome: comparison to children with Down syndrome. Genetics in Medicine 2001; 3: 72–78
  • Shprintzen R. J., Goldberg R. B., Lewin M. L., Sidoti E. J., Berkman M. D., Argamaso R. V., Young D. A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: Velo‐Cardio‐Facial Syndrome. Cleft palate Journal 1978; 5: 56–62
  • Shprintzen R. J., Goldberg R. B., Young D., Wolford L. The Velo‐cardio‐facial syndrome: a clinical and genetic analysis. Pediatrics 1981; 67: 167–172
  • Solot C. B., Gerdes M., Kirschner R. E., McDonald‐McGinn D. M., Moss E., Woodin M., Aleman D., Zackai E. H., Wang P. P. Communication issues in 22q11. 2 deletion syndrome: children at risk. Genetics in Medicine 2001; 3: 67–71
  • Solot C. B., Knightly C., Handler S. D., Gerdes M., McDonald‐McGinn D. M., Moss E., Wang P., Cohen M., Randall P., La Rossa D., Driscoll D. A., Emanuel B. S., Zackai E. H. Communication disorders in the 22q11. 2 microdeletion syndrome. Journal of Communication Disorders 2000; 33: 187–204
  • Stothard S. E., Snowling M. J., Bishop D. V. M., Chipchase B. B., Kaplan C. A. Language‐impaired preschoolers: a follow‐up into adolescence. Journal of Speech, Language, and Hearing Research 1998; 41: 407–418
  • Svensson Y., Tuominen‐Eriksson A. ‐M. Buss‐sagan. Specialpedagogiska institutet Läromedel, Umea 2002
  • Swillen A., Devriendt K., Legius E., Eyskens B., Dumoulin M., Gewillig M., Fryns J. P. Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 37 children and adolescents with VCFS. Journal of Medical Genetics 1997; 34: 453–458
  • Swillen A., Devriendt K., Legius E., Prinzie P., Vogels A., Ghesquière P., Fryns J. P. The behavioural phenotype in velo‐cardio‐facial syndrome (VCFS): from infancy to adolescence. Genetic Counseling 1999; 10: 79–88
  • Swillen A., Devriendt K., Van Trappen G., Vogels A., Rommel N., Fryns J. ‐P., Eyskens B., Gewillig M., Dumoulin M. Familial deletions of chromosome 22q11. American Journal of Medical Genetics 1998; 80: 531–532
  • Westerlund M. Barn med tal‐ och språkavvikelser. 1994, Doctoral thesis, Uppsala University, Uppsala
  • Yamagishi H. The 22q11.2 deletion syndrome. Keio Journal of Medicine 2002; 51: 77–88

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.