کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
3037181 | 1184403 | 2012 | 4 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Searching for Potocki–Lupski syndrome phenotype: A patient with language impairment and no autism
دانلود مقاله + سفارش ترجمه
دانلود مقاله ISI انگلیسی
رایگان برای ایرانیان
موضوعات مرتبط
علوم زیستی و بیوفناوری
علم عصب شناسی
علوم اعصاب تکاملی
پیش نمایش صفحه اول مقاله

چکیده انگلیسی
Potocki–Lupski syndrome (PTLS; OMIM 610883) is a genomic syndrome that arises as a result of a duplication of 17p11.2. Although numerous cases of individuals with PTLS have been presented in the literature, its behavioral characterization is still ambiguous. We present a male child with a de novo dup(17)(p11.2p11.2) and he does not possess any autistic features, but is characterized by severe speech and language impairment. In the context of the analyses of this patient and other cases of PTLS, we argue that the central feature of the syndrome appears to be related to diminished speech and language capacity, rather than the specific social deficits central to autism.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Brain and Development - Volume 34, Issue 8, September 2012, Pages 700–703
Journal: Brain and Development - Volume 34, Issue 8, September 2012, Pages 700–703
نویسندگان
A. Gulhan Ercan-Sencicek, Nicole R. Davis Wright, Stephen J. Frost, Robert K. Fulbright, Susan Felsenfeld, Lesley Hart, Nicole Landi, W. Einar Mencl, Stephan J. Sanders, Kenneth R. Pugh, Matthew W. State, Elena L. Grigorenko,