دانلود مقاله ISI انگلیسی شماره 75610
عنوان فارسی مقاله

اشکال اولیه اجتماعی و ارتباطی و توابع در سندرم رت معمولی

کد مقاله سال انتشار مقاله انگلیسی ترجمه فارسی تعداد کلمات
75610 2013 6 صفحه PDF سفارش دهید محاسبه نشده
خرید مقاله
پس از پرداخت، فوراً می توانید مقاله را دانلود فرمایید.
عنوان انگلیسی
Early socio-communicative forms and functions in typical Rett syndrome
منبع

Publisher : Elsevier - Science Direct (الزویر - ساینس دایرکت)

Journal : Research in Developmental Disabilities, Volume 34, Issue 10, October 2013, Pages 3133–3138

کلمات کلیدی
فیلم خانواده؛ فیلم های خانگی؛ نوزادان؛ تجزیه و تحلیل گذشته نگر؛ سندرم رت؛ توسعه اجتماعی و ارتباطی؛ تجزیه و تحلیل ویدئویی
پیش نمایش مقاله
پیش نمایش مقاله اشکال اولیه اجتماعی و ارتباطی و توابع در سندرم رت معمولی

چکیده انگلیسی

Rett syndrome (RTT) is a severe neurological disorder characterized by a developmental regression in motor and speech-language domains. There is, however, limited research on socio-communicative development of affected children before the onset of regression. We analyzed audio–video recordings made by parents of six 9- to 12-month old girls later diagnosed with typical RTT, applying the Inventory of Potential Communicative Acts (IPCA) to identify early communicative forms and functions. Each girl used at least one communicative form (e.g., body movement, eye gaze, or vocalizations) to gain attention and answer, but none were observed to make choices or request information. Varying numbers of children were observed to perform other communicative functions according to the IPCA including social convention, rejecting or requesting an object. Non-verbal forms (e.g., reaching, moving closer, eye contact, smiling) were more common than non-linguistic verbal forms (e.g., unspecified vocalizations, pleasure vocalizations, crying). (Pre-)linguistic verbal forms (e.g., canonical or variegated babbling, proto-words) were not used for communicative purposes. These data suggest that atypical developmental patterns in the socio-communicative domain are evident prior to regression in young individuals later diagnosed with RTT.

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