Down syndrome

dc.contributor.authorAydin, Mustafa
dc.contributor.authorKabakuş, Nimet
dc.contributor.authorÖzcan, Kenan
dc.contributor.authorTaşkin, Erdal
dc.contributor.authorÖzlü, Ferda
dc.date.accessioned2026-08-12T16:11:08Z
dc.date.issued2006
dc.departmentFırat Üniversitesi
dc.description.abstractDown syndrome is a genetic disorder with an excess genetic material on 21th chromosome, mild mental retardation and anomalies of multiple organ systems. Physical and neurophysicological findings such as mental retardation, linguistic and memory problems accompany this syndrome. Neuroanatomical origins of this cognitive dysfunctions are not clear yet. The risk of Down syndrome differs with respect to races, and ethnic groups, maternal age distribution, prenatal diagnosis and cytogenetic analysis.
dc.identifier.endpage44
dc.identifier.issn1016-5134
dc.identifier.issue7
dc.identifier.scopus2-s2.0-33747620726
dc.identifier.scopusqualityN/A
dc.identifier.startpage38
dc.identifier.urihttps://hdl.handle.net/11508/42317
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.subjectchromosome 21; chromosome translocation; cytogenetics; Down syndrome; ethnology; human; language ability; maternal age; memory disorder; mental deficiency; prenatal diagnosis; review; risk assessment
dc.titleDown syndrome
dc.title.alternativeDown sendromu
dc.typeReview Article

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