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Auteur P. KATERINA |
Documents disponibles écrits par cet auteur (1)



Autism Spectrum Disorder and Psychiatric Comorbidity in a Patient with Myhre Syndrome / P. ARTEMIOS in Journal of Autism and Developmental Disorders, 49-7 (July 2019)
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Titre : Autism Spectrum Disorder and Psychiatric Comorbidity in a Patient with Myhre Syndrome Type de document : Texte imprimé et/ou numérique Auteurs : P. ARTEMIOS, Auteur ; S. ARETI, Auteur ; P. KATERINA, Auteur ; F. HELEN, Auteur ; T. EIRINI, Auteur ; P. CHARALAMBOS, Auteur Article en page(s) : p.3031-3035 Langues : Anglais (eng) Mots-clés : Affective disorder High functioning autism spectrum disorder Myhre syndrome SMAD4 mutation Index. décimale : PER Périodiques Résumé : Myhre syndrome (MS) is a connective tissue disorder with multisystem involvement with or without intellectual disability. In most cases SMAD4 mutations are reported. To date, 55 individuals have been molecularly confirmed. Autism has been proposed among associate clinical features of MS but no standardized diagnosis was available in previous cases. We report a case of a 25-year-old man with a pathogenic heterozygous SMAD4 missense mutation affecting residue Arg(496) (SMAD4:p.Arg496Cys). Clinical findings are consistent with MS, commorbid with affective disorder and High Functioning Autism Spectrum Disorder confirmed by a standardized assessment procedure. The thorough clinical assessment of cases with syndromes such as MS can extend our knowledge on both the phenotypic characteristics of the syndrome and the genetic basis of autism. En ligne : http://dx.doi.org/10.1007/s10803-019-04015-y Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=402
in Journal of Autism and Developmental Disorders > 49-7 (July 2019) . - p.3031-3035[article] Autism Spectrum Disorder and Psychiatric Comorbidity in a Patient with Myhre Syndrome [Texte imprimé et/ou numérique] / P. ARTEMIOS, Auteur ; S. ARETI, Auteur ; P. KATERINA, Auteur ; F. HELEN, Auteur ; T. EIRINI, Auteur ; P. CHARALAMBOS, Auteur . - p.3031-3035.
Langues : Anglais (eng)
in Journal of Autism and Developmental Disorders > 49-7 (July 2019) . - p.3031-3035
Mots-clés : Affective disorder High functioning autism spectrum disorder Myhre syndrome SMAD4 mutation Index. décimale : PER Périodiques Résumé : Myhre syndrome (MS) is a connective tissue disorder with multisystem involvement with or without intellectual disability. In most cases SMAD4 mutations are reported. To date, 55 individuals have been molecularly confirmed. Autism has been proposed among associate clinical features of MS but no standardized diagnosis was available in previous cases. We report a case of a 25-year-old man with a pathogenic heterozygous SMAD4 missense mutation affecting residue Arg(496) (SMAD4:p.Arg496Cys). Clinical findings are consistent with MS, commorbid with affective disorder and High Functioning Autism Spectrum Disorder confirmed by a standardized assessment procedure. The thorough clinical assessment of cases with syndromes such as MS can extend our knowledge on both the phenotypic characteristics of the syndrome and the genetic basis of autism. En ligne : http://dx.doi.org/10.1007/s10803-019-04015-y Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=402