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Germ Cell Tumor Showing Partial Trisomy 1 in a Gonadectomized Intersex Child with Monosomy X and Double Y Mosaicism

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dc.authorscopusid55402094800
dc.authorscopusid8876487000
dc.authorscopusid6602111071
dc.authorscopusid6602003464
dc.authorscopusid15070170300
dc.authorscopusid12139290200
dc.authorscopusid18038773000
dc.contributor.authorOgǔr, G.
dc.contributor.authorPinarli, F.G.
dc.contributor.authorDaǧdemir, A.
dc.contributor.authorArtan, S.
dc.contributor.authorArtürk, E.
dc.contributor.authorElli, M.
dc.contributor.authorSezer, Ö.
dc.date.accessioned2020-06-21T15:25:09Z
dc.date.available2020-06-21T15:25:09Z
dc.date.issued2006
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Ogǔr] Gönül, Department of Pediatric Genetics, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Pinarli] Faruk Guclu, Department of Pediatric Oncology, Ondokuz Mayis Üniversitesi, Samsun, Turkey, Department of Pediatric Oncology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Daǧdemir] Ayhan, Department of Pediatric Oncology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Artan] Sevilhan, Department of Medical Genetics, Eskişehir Osmangazi Üniversitesi, Eskisehir, Eskisehir, Turkey; [Artürk] Ender, Department of Pediatric Surgery, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Elli] Murat, Department of Pediatric Oncology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Sezer] Ozlem Türkeli, Department of Medical Biology and Genetics, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Ökten] Gülsen, Department of Medical Biology and Genetics, Ondokuz Mayis Üniversitesi, Samsun, Turkeyen_US
dc.description.abstractHigh incidence of germ cell tumors arising from dysgenetic gonads in patients with sexual chromosome abnormalities has been described, especially in patients with a Y chromosome bearing cell line. Here we report a 14-year-old patient with ambiguous genitalia. Constitutional karyotype showed 45,X/46,X,derY [?t(Yp;Yq)] mosaicism. The patient developed an abdominally located mixed malignant germ cell tumor 5 years after the removal of the dysgenetic gonads. Tumor karyotype showed partial trisomy 1q, a derivative 8q, and a hyperdiploidy with +X, +7, +12, +15, +19, +21, and an unidentified marker. © 2006 Lippincott Williams & Wilkins, Inc.en_US
dc.identifier.doi10.1097/01.mph.0000243651.33561.d4
dc.identifier.endpage754en_US
dc.identifier.issn1077-4114
dc.identifier.issn1536-3678
dc.identifier.issue11en_US
dc.identifier.pmid17114963
dc.identifier.scopus2-s2.0-33751205631
dc.identifier.scopusqualityQ3
dc.identifier.startpage750en_US
dc.identifier.urihttps://doi.org/10.1097/01.mph.0000243651.33561.d4
dc.identifier.volume28en_US
dc.identifier.wosWOS:000242505800009
dc.identifier.wosqualityQ3
dc.language.isoenen_US
dc.publisherLippincott Williams & Wilkinsen_US
dc.relation.ispartofJournal of Pediatric Hematology Oncologyen_US
dc.relation.journalJournal of Pediatric Hematology Oncologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCytogeneticsen_US
dc.subjectDouble Y Chromosomeen_US
dc.subjectGerm Cell Tumoren_US
dc.subjectGonadal Dysgenesisen_US
dc.titleGerm Cell Tumor Showing Partial Trisomy 1 in a Gonadectomized Intersex Child with Monosomy X and Double Y Mosaicismen_US
dc.typeArticleen_US
dspace.entity.typePublication

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