Atıf İçin Kopyala
ALANAY Y., Unal F., Turanli G., Alikasifoglu M., Alehan D., Akyol U., ...Daha Fazla
JOURNAL OF INTELLECTUAL DISABILITY RESEARCH, cilt.51, ss.151-161, 2007 (SCI-Expanded)
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Yayın Türü:
Makale / Tam Makale
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Cilt numarası:
51
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Basım Tarihi:
2007
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Doi Numarası:
10.1111/j.1365-2788.2006.00942.x
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Dergi Adı:
JOURNAL OF INTELLECTUAL DISABILITY RESEARCH
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Derginin Tarandığı İndeksler:
Science Citation Index Expanded (SCI-EXPANDED), Social Sciences Citation Index (SSCI), Scopus
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Sayfa Sayıları:
ss.151-161
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Anahtar Kelimeler:
fragile X, intellectual disability, multidisciplinary approach, EEG FINDINGS, EPILEPSY, BEHAVIOR, CHILDREN, MALES, ATTENTION, DEFICITS, AUTISM, BOYS
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Hacettepe Üniversitesi Adresli:
Evet
Özet
Background: Fragile X syndrome (FXS) is the most common inherited form of intellectual disability. Since the identification of the responsible gene (FMR1) and its protein (FMRP), there has been enormous progress in both clinical and pathogenetic research on the neurobehavioural aspects of the condition. However, studies regarding other medical problems anticipated in individuals with FXS are limited. A multidisciplinary study evaluating various causes of morbidity in the same group has not been published yet.