The diagnosis of autism in a female: Could it be Rett syndrome?

Deidra J. Young, Ami Bebbington, Alison Anderson, David Ravine, Carolyn Ellaway, Alpana Kulkarni, Nick De Klerk, Walter E. Kaufmann, Helen Leonard

    Research output: Contribution to journalArticlepeer-review


    The overlap between autism and Rett syndrome clinical features has led to many cases of Rett syndrome being initially diagnosed with infantile autism or as having some autistic features. Both conditions seriously disrupt social and language development and are often accompanied by repetitive, nonpurposeful stereotypic hand movements. The aims of this study were to compare the early and subsequent clinical courses of female subjects with Rett syndrome categorised by whether or not a diagnosis of autism had been proposed before Rett syndrome had been diagnosed and compare the spectrum of methyl-CpG binding protein 2 (MECP2) mutations identified among the two groups. This study made use of a total of 313 cases recorded in two databases: the Australian Rett Syndrome Database (ARSD) and the International Rett Syndrome Phenotype Database (InterRett). Cases with an initial diagnosis of autism had significantly milder Rett syndrome symptoms and were more likely to remain ambulant, to have some functional hand use and not to have developed a scoliosis. Females with the p.R306C or p.T158M mutations in the MECP2 gene were more likely to have an initial diagnosis of autism, and the specific Rett syndrome symptoms were noted at a later age. We recommend that females who are initially considered to have autism be carefully monitored for the evolution of the signs and symptoms of Rett syndrome.

    Original languageEnglish (US)
    Pages (from-to)661-669
    Number of pages9
    JournalEuropean Journal of Pediatrics
    Issue number6
    StatePublished - Jun 2008


    • Autism
    • Autistic spectrum disorders
    • MECP2
    • Rett syndrome

    ASJC Scopus subject areas

    • Pediatrics, Perinatology, and Child Health

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