Publication:
A Case with Down Syndrome Presenting 21q22q Translocation: Differential Diagnosis

dc.authorscopusid6603432100
dc.authorscopusid6603455076
dc.authorscopusid6701800423
dc.authorscopusid7003539720
dc.authorscopusid18038193800
dc.authorscopusid23471430800
dc.authorscopusid23471430800
dc.contributor.authorGüneş, S.
dc.contributor.authorKara, N.
dc.contributor.authorGünal, N.
dc.contributor.authorKüçüködük, Ş.
dc.contributor.authorÖkten, G.
dc.contributor.authorTural, Ş.
dc.contributor.authorTaşkin, E.
dc.date.accessioned2025-12-10T21:20:59Z
dc.date.issued2007
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Güneş] Sezgin Özgür, Tibbi Genetik BD, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Kara] Nurten, Tibbi Genetik BD, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Günal] Nazlihan, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Küçüködük] Şükrü, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Ökten] Gülsen, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Tural] Şengül, Tibbi Genetik BD, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Taşkin] Emre, Tibbi Genetik BD, Ondokuz Mayis Üniversitesi, Samsun, Turkeyen_US
dc.description.abstractRobertsonian translocations (ROBs) are the most common chromosomal rearrangemets. ROBs are whole-arm rearrangements between the acrocentric chromosomes chromosomes 13, 14, 15, 21, and 22. ROBs can be classified into 2 groups depending on their frequency of occurrence, common [rob(13q14q) and rob(14q21q)] and rare (all remaining possible nonhomologous combinations). Each of the rare types make up only 0.8% to 3.7% of the total number of ROBs. ROBs involving chromosome 21 are found in approximately 5% of patients with Down syndrome (DS). The most common nonhomologous ROB in DS is rob(14q21q). Rob(21q;22q) is an uncommon ROB. In this case a 4-year-old boy with 21q22q translocation is discussed briefly. The literature about ROBs was reviewed. Copyright © 2007 by Türkiye Klinikleri.en_US
dc.identifier.endpage929en_US
dc.identifier.issn1300-0292
dc.identifier.issue6en_US
dc.identifier.scopus2-s2.0-38349084807
dc.identifier.scopusqualityQ4
dc.identifier.startpage928en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12712/34628
dc.identifier.volume27en_US
dc.identifier.wosqualityN/A
dc.language.isotren_US
dc.publisherTürkiye Kliniklerien_US
dc.relation.ispartofTurkiye Klinikleri Journal of Medical Sciencesen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectDown Syndromeen_US
dc.subjectTranslocation, Geneticen_US
dc.titleA Case with Down Syndrome Presenting 21q22q Translocation: Differential Diagnosisen_US
dc.title.alternative21q22q Translokasyonu Saptanan Bir Down Sendromu Olgusuen_US
dc.typeArticleen_US
dspace.entity.typePublication

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