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Autism, language delay and mental retardation in a patient with 7q11 duplication
  1. Christel Depienne
  1. INSERM U679, France
    1. Delphine Heron
    1. Département de Génétique, Cytogénétique et Embryologie, France
      1. Catalina Betancur
      1. INSERM U513, France
        1. Baya Benyahia
        1. Département de Génétique, Cytogénétique et Embryologie, France
          1. Oriane Trouillard
          1. Département de Génétique, Cytogénétique et Embryologie, France
            1. Delphine Bouteiller
            1. INSERM U679, France
              1. Alain Verloes
              1. Département de Génétique, Hôpital Robert Debré, France
                1. Eric LeGuern
                1. INSERM U679, France
                  1. Marion Leboyer
                  1. INSERM U513, France
                    1. Alexis Brice (brice{at}
                    1. INSERM U679, France


                      Background: Chromosomal rearrangements, arising from unequal recombination between repeated sequences, are found in a subset of patients with autism. Duplications involving loci associated with behavioural disturbances especially constitute a good candidate mechanism. The Williams-Beuren Critical Region (WBCR), located in 7q11.23, is commonly deleted in the Williams-Beuren microdeletion syndrome (WBS). However, only four patients with a duplication of the WBCR have been reported so far, one with severe language delay and the three others with variable developmental, psychomotor and language delay.

                      Objective and Methods: In this study, we screened 206 patients with autism spectrum disorders for the WBCR duplication by quantitative microsatellite analysis and multiple ligation-dependent probe amplification (MLPA).

                      Results: We have identified one male patient with a de novo interstitial duplication of the entire WBCR of paternal origin. The patient had autistic disorder, severe language delay and mental retardation, with very mild dysmorphic features.

                      Conclusion: We report the first patient with autistic disorder who has a WBCR duplication. This observation indicates that the 7q11.23 duplication could be involved in complex clinical phenotypes, ranging from developmental or language delay to mental retardation and autism, and extends the phenotype initially reported. These findings also support the existence of one or several genes in 7q11.23 sensitive to gene dosage and involved in the development of language and social interactions.

                      • 7q11
                      • Autism
                      • duplication
                      • language delay
                      • mental retardation

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