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- W2404741595 abstract "No AccessJournal of Urology1 Sep 1991Chromosomal Anomaly and Malformation Syndrome with Abdominal Polyorchidism Fiorella Shabtai, A. Schwartz, J. Hart, I. Halbrecht, and David Kimche Fiorella ShabtaiFiorella Shabtai More articles by this author , A. SchwartzA. Schwartz More articles by this author , J. HartJ. Hart More articles by this author , I. HalbrechtI. Halbrecht More articles by this author , and David KimcheDavid Kimche More articles by this author View All Author Informationhttps://doi.org/10.1016/S0022-5347(17)37934-XAboutPDF ToolsAdd to favoritesDownload CitationsTrack CitationsPermissionsReprints ShareFacebookLinked InTwitterEmail We describe a neonate who presented with multiple severe malformations including polyorchidism. To our knowledge this is the second case reported with ipsilateral testes located intra-abdominally. Chromosomal studies in cases of polyorchidism have been reported previously only once and the patient exhibited a normal karyotype. Our patient had a chromosome 21 long arm deletion. Interestingly, a trisomy 21 patient has been reported with agonadism. We suggest that genes on chromosome 21 may have some role in gonadal development. © 1991 by The American Urological Association Education and Research, Inc.FiguresReferencesRelatedDetails Volume 146Issue 3September 1991Page: 833-834 Advertisement Copyright & Permissions© 1991 by The American Urological Association Education and Research, Inc.Keywordsabnormalitiestestisurogenital systemchromosomes, human, pair 21MetricsAuthor Information Fiorella Shabtai More articles by this author A. Schwartz More articles by this author J. Hart More articles by this author I. Halbrecht More articles by this author David Kimche More articles by this author Expand All Advertisement Loading ..." @default.
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- W2404741595 date "1991-09-01" @default.
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- W2404741595 title "Chromosomal Anomaly and Malformation Syndrome with Abdominal Polyorchidism" @default.
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