Autistic-Like Traits in Pena-Shokeir Syndrome / M. KALINLI in Journal of Autism and Developmental Disorders, 49-3 (March 2019)  

Public ISBD [article]  inJournal of Autism and Developmental Disorders > 49-3 (March 2019) . - p.1316-1318 Titre : Autistic-Like Traits in Pena-Shokeir Syndrome Type de document : texte imprimé Auteurs : M. KALINLI, Auteur ; Özalp EKINCI, Auteur ; S. GUNES, Auteur ; Nuran EKINCI, Auteur Article en page(s) : p.1316-1318 Langues : Anglais (eng) Mots-clés : Autism  Autistic traits  Pena-Shokeir syndrome Index. décimale : PER Périodiques Résumé : Pena-Shokeir syndrome (PSS) is a rare, early lethal disease. PSS is characterized by fetal growth restriction, craniofacial deformities, multiple ankyloses and pulmonary hypoplasia. Because of the primary concern of physical health problems, psychiatric evaluation is frequently underestimated in PSS patients. Our case report describes a child with PSS who presented with autistic spectrum disorder symptoms. En ligne : http://dx.doi.org/10.1007/s10803-018-3824-2 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=386 [article] Autistic-Like Traits in Pena-Shokeir Syndrome [texte imprimé] / M. KALINLI, Auteur ; Özalp EKINCI, Auteur ; S. GUNES, Auteur ; Nuran EKINCI, Auteur . - p.1316-1318. Langues : Anglais (eng) in Journal of Autism and Developmental Disorders > 49-3 (March 2019) . - p.1316-1318 Mots-clés : Autism  Autistic traits  Pena-Shokeir syndrome Index. décimale : PER Périodiques Résumé : Pena-Shokeir syndrome (PSS) is a rare, early lethal disease. PSS is characterized by fetal growth restriction, craniofacial deformities, multiple ankyloses and pulmonary hypoplasia. Because of the primary concern of physical health problems, psychiatric evaluation is frequently underestimated in PSS patients. Our case report describes a child with PSS who presented with autistic spectrum disorder symptoms. En ligne : http://dx.doi.org/10.1007/s10803-018-3824-2 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=386

Coexistence of 9p Deletion Syndrome and Autism Spectrum Disorder / Serkan GÃœNES in Journal of Autism and Developmental Disorders, 47-2 (February 2017)  

Public ISBD [article]  inJournal of Autism and Developmental Disorders > 47-2 (February 2017) . - p.520-521 Titre : Coexistence of 9p Deletion Syndrome and Autism Spectrum Disorder Type de document : texte imprimé Auteurs : Serkan GÃœNES, Auteur ; Özalp EKINCI, Auteur ; Nuran EKINCI, Auteur ; Fevziye TOROS, Auteur Article en page(s) : p.520-521 Langues : Anglais (eng) Mots-clés : 9p  Deletion  Autism Index. décimale : PER Périodiques Résumé : Deletion or duplication of the short arm of chromosome 9 may lead to a variety of clinical conditions including craniofacial and limb abnormalities, skeletal malformations, mental retardation, and autism spectrum disorder. Here, we present a case report of 5-year-old boy with 9p deletion syndrome and autism spectrum disorder. En ligne : http://dx.doi.org/10.1007/s10803-016-2943-x Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=303 [article] Coexistence of 9p Deletion Syndrome and Autism Spectrum Disorder [texte imprimé] / Serkan GÃœNES, Auteur ; Özalp EKINCI, Auteur ; Nuran EKINCI, Auteur ; Fevziye TOROS, Auteur . - p.520-521. Langues : Anglais (eng) in Journal of Autism and Developmental Disorders > 47-2 (February 2017) . - p.520-521 Mots-clés : 9p  Deletion  Autism Index. décimale : PER Périodiques Résumé : Deletion or duplication of the short arm of chromosome 9 may lead to a variety of clinical conditions including craniofacial and limb abnormalities, skeletal malformations, mental retardation, and autism spectrum disorder. Here, we present a case report of 5-year-old boy with 9p deletion syndrome and autism spectrum disorder. En ligne : http://dx.doi.org/10.1007/s10803-016-2943-x Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=303

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