Childhood autism and associated comorbidities

Autism is a heterogeneous neurodevelopmental disorder with a variety of different etiologies, but with a heritability estimate of more than 90%. Although the strong correlation between autism and genetic factors has been long established, the exact genetic background of autism is still unclear. This...

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Published inBrain & development Vol. 29; no. 5; pp. 257 - 272
Main Authors Zafeiriou, Dimitrios I., Ververi, Athena, Vargiami, Euthymia
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.06.2007
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ISSN0387-7604
1872-7131
DOI10.1016/j.braindev.2006.09.003

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Summary:Autism is a heterogeneous neurodevelopmental disorder with a variety of different etiologies, but with a heritability estimate of more than 90%. Although the strong correlation between autism and genetic factors has been long established, the exact genetic background of autism is still unclear. This review refers to all the genetic syndromes that have been described in children with pervasive developmental disorders (tuberous sclerosis, fragile X, Down, neurofibromatosis, Angelman, Prader-Willi, Gilles de la Tourette, Williams, etc.). Issues covered include prevalence and main characteristics of each syndrome, as well as the possible base of its association with autism in terms of contribution to the current knowledge on the etiology and genetic base of pervasive developmental disorders.
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ISSN:0387-7604
1872-7131
DOI:10.1016/j.braindev.2006.09.003