Mental retardation and fragil X syndrome

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dc.contributor.authorAydin, Mustafa
dc.contributor.authorTaşkin, Erdal
dc.contributor.authorÖzcan, Kenan
dc.contributor.authorKabakuş, Nimet
dc.contributor.authorÖzlü, Ferda
dc.date.accessioned2026-08-12T16:11:07Z
dc.date.issued2006
dc.departmentFırat Üniversitesi
dc.description.abstractFragile X syndrome is a genetic disorder with a semidominance of X chromosome due to mutation in fragile X mental retardation-1 gen (familial mental retardation-1 or FMR-1) which is characterized by learning, linguistic and memory problems due to temporal lobe dysfunction. Fragile X syndrome is the second common cause of mental retardation after Down syndrome. Fragile X syndrome constitues 1/3-1/4 of X linked mental retardation. Its incidence is 1/4000 in male, 1/6000 in female children. There is no difference between ethnic groups.
dc.identifier.endpage42
dc.identifier.issn1016-5134
dc.identifier.issue9
dc.identifier.scopus2-s2.0-33750946975
dc.identifier.scopusqualityN/A
dc.identifier.startpage37
dc.identifier.urihttps://hdl.handle.net/11508/42315
dc.identifier.volume18
dc.indekslendigikaynakScopus
dc.language.isotr
dc.relation.ispartofSENDROM
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_Scopus_20260511
dc.subjectbrain dysfunction; chromosome mutation; clinical feature; Down syndrome; fragile X syndrome; human; mental deficiency; morbidity; review; sex ratio; temporal lobe; X chromosome
dc.titleMental retardation and fragil X syndrome
dc.title.alternativeMental retardasyon ve frajil X sendromu
dc.typeReview Article

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