Asperger Syndrome Associated with Steinert's Myotonic Dystrophy'

Abstract

Developmental Medicine & Child NeurologyVolume 39, Issue 4 p. 280-281 Free Access Asperger Syndrome Associated with Steinert's Myotonic Dystrophy' First published: 29 September 2008 https://doi.org/10.1111/j.1469-8749.1997.tb07430.xAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinkedInRedditWechat No abstract is available for this article. References Aslandis C., Jansen G., Amemiya C., Shutler G., Mahadevan M., Tsilfidis C., Chen C., Alleman J., Wormskamp NGM, Vooijs M. et al. (1992) Cloning of the essential myotonie dystrophy region and mapping of the putative defect. Nature 355: 548– 51. Asperger H.. (1979) Problems of infantile autism, Communication 13: 45– 52. Blondis TA, Cook Jr E., Koza-Taylor P., Finn T.. (1996) Asperger Syndrome associated with Steinert's Myotonic Dystrophy. Developmental Medicine and Child Neurology 38: 840– 7. Buxton J., Shelbourne P., Davies J., Jones C., van Tongeren T., Aslandis C., de Jong P., Jansen G., Anvret M., Riley B., et al. (1992) Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy. Nature 365: 547– 8. Harley H., Brook JD, Rundle SA, Crow S., Reardon W., Buckler AJ, Harper PS, Housman DE, Shaw DJ. (1992) Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy. Nature 355: 545– 6. Harley H., Rundle SA, MacMillan JC, Myring J., Brook JD, Crow S., Reardon W., Fenton I., Shaw DJ, Harper PS. (1993) Size of the unstable CTG sequence in relation to phenotype and parpntal transmission in myotonic dystrophy. American Journal of Human Genetics 52: 1164– 74. Hunter A., Tsilfidis C., Mettler G., Jacpb P., Mahadevan M., Surh L., Korneluk R.. (1992) The correlation of age of onset with CTG trinucleotide repeat amplification in Myotonic dystrophy. Journal of Medical Genetics 29: 774– 8. Koch MC, Grimm T., Harley HG, Harper PS. (1991) Genetic risks for children of women with myotonic dystrophy. American Journal of Human Genetics 48: 1084– 91. Turnpenny P., Clark C., Kelly K.. (1994) Intelligence quotient profile in myotonic dystrophy, intergenerational deficit, and correlation with CTG amplification. Journal of Medical Genetics 31: 300– 5. van Krevelen DA. (1971) Early infantile autism and autistic psychopath. Journal of Autism and Childhood Schizophrenia 1: 82– 6. Wing L., Gould J.. (1979) Severe impairments of social interaction and. associated abnormalities in children: Epidemiology and classification. Journal of Autism and Developmental Disorders 9: 11– 29. World Health Organization (1992) The ICD 10 Classification of Mental and Behavioural Disorders. Geneva : WHO. Yoshimura I., Sasaki A., Akimoto H., Yoshimura N.. (1989) A case of congenital myotonic dystrophy with infantile autism. No To Haltalsu 21: 379– 84. Volume39, Issue4April 1997Pages 280-281 ReferencesRelatedInformation