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Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/24817
Title: Severe hypospadias associated with Robertsonian translocation
Authors: Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Cerrahisi Anabilim Dalı.
Uludağ Üniversitesi/Tıp Fakültesi/Pediatrik Endokrinoloji Anabilim Dalı.
Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Genetik Anabilim Dalı.
Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Cerrahisi ve Çocuk Ürolojisi Anabilim Dalı.
0000-0003-0710-5422
Kılıç, Nizamettin
Balkan, Emin
Sağlam, Halil
Yakut, Tahsin
Doǧruyol, Hasan
AAI-3656-2021
C-7392-2019
7005266570
7004109012
35612700100
6602802424
56624750400
Keywords: Urology & nephrology
Hypospadias
Robertsonian translocation
Amniocentesis
Carriers
Rearrangements
Rates
Issue Date: 2005
Publisher: Karger
Citation: Kılıç, N. vd. (2005). "Severe hypospadias associated with Robertsonian translocation". Urologia Internationalis, 74(4), 373-376.
Abstract: In this study, we report a 3-year-old boy with severe scrotal hypospadias with Robertsonian translocation [45, XY, t(13q;14q)]. The patient was born at term with a low birth weight and hypospadias. There was no endocrinological abnormality. His father also has a balanced 13-14 Robertsonian translocation. Two-stage hypospadias repair was carried out. The presence of this chromosomal anomaly and hypospadias are unique to our patient, compared to others with the 45, XY, t( 13q; 14q) translocation. Although no such association has been reported so far, we thought that severe hypospadias in this case might be associated with this translocation.
URI: https://doi.org/10.1159/000084443
https://www.karger.com/Article/Abstract/84443
http://hdl.handle.net/11452/24817
ISSN: 0042-1138
1423-0399
Appears in Collections:Scopus
Web of Science

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