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Infant with MCA and severe cutis laxa due to a de novo duplication 11p of paternal origin

Authors

  • T. Gardeitchik,

    1. Department of Pediatrics, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands
    2. Institute for Genetic and Metabolic Diseases, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands
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  • N. de Leeuw,

    1. Department of Human Genetics, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands
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  • L. Nijtmans,

    1. Department of Pediatrics, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands
    2. Institute for Genetic and Metabolic Diseases, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands
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  • P. Jira,

    1. Jeroen Bosch Hospital, s' Hertogenbosch, The Netherlands
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  • T. Kozicz,

    1. Department of Cellular Animal Physiology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Nijmegen, Nijmegen, The Netherlands
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  • M. Czako,

    1. Department of Medical Genetics, University of Pecs, Pecs, Hungary
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  • I. van de Burgt,

    1. Department of Human Genetics, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands
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  • E. Morava

    Corresponding author
    1. Department of Pediatrics, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands
    2. Institute for Genetic and Metabolic Diseases, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands
    • Department of Pediatrics, Institute for Genetic and Metabolic Diseases, Radboud University Nijmegen Medical Centre, Nijmegen, P.O Box 9101, 6500 HB Nijmegen, The Netherlands.
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  • All authors declare that there are no conflicts of interest.

  • How to Cite this Article: Gardeitchik T, de Leeuw N, Nijtmans L, Jira P, Kozicz T, Czako M, van de Burgt I, Morava E. 2012. Infant with MCA and severe cutis laxa due to a de novo duplication 11p of paternal origin. Am J Med Genet Part A 158A:469–472.

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