Les objectifs étaient de décrire les caractéristiques démographiques des enfants ayant le syndrome du X fragile (SXF) et de déterminer les prédicteurs de la fréquentation de cliniques pour le X fragile (XF). Les résultats provenant des échantillons du Community Support Network (CSN) et du Our Fragile X World (OFXW) ont montré que les enfants qui ont fréquenté les cliniques pour le XF étaient principalement de sexe masculin, d'âge du secondaire ou plus jeunes, blancs et non-hispaniques. En utilisant des modèles de régression logistique, la sensibilisation aux services offerts par les cliniques pour le XF, l'éducation et le revenu du responsable légal (CSN), ainsi que l'âge de l'enfant, le revenu familial et le nombre total de troubles concomitants (OFXW) étaient des prédicteurs de la fréquentation des cliniques. Les caractéristiques démographiques et celles des enfants représentaient une grande partie de la variance expliquée. De manière importante, la sévérité des symptômes et la...
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1 November 2017
Research Article|
November 01 2017
Résumés en Français
Am J Intellect Dev Disabil (2017) 122 (6): 561–562.
Citation
Résumés en Français. Am J Intellect Dev Disabil 1 November 2017; 122 (6): 561–562. doi: https://doi.org/10.1352/1944-7558-122.6.561
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