Embryology of the Absent Vas Supported by 2 Cases of Congenital Unilateral Absence of Vas With Varied Associations
Congenital absence of the vas occurs in up to 1% of men. Congenital unilateral absence of the vas deferens can be related to cystic fibrosis transmembrane conductance regulator mutations or in 79% of cases, renal agenesis. We present a case of each, diagnosed in children at operation for elective in...
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doaj-70653facb784423c9ed1216bbe588ae12020-11-25T00:45:00ZengElsevierUrology Case Reports2214-44202014-03-01224950Embryology of the Absent Vas Supported by 2 Cases of Congenital Unilateral Absence of Vas With Varied AssociationsGregory Shepherd0Ashok Rajimwale1Department of Paediatric Urology, Nottingham Children's Hospital, Queen's Medical Centre, Nottingham, UK; Corresponding author. Tel.: +44 787929846; fax: +44 116 2587637Department of Paediatric Urology, The Children's Hospital, Leicester Royal Infirmary, Leicester, UKCongenital absence of the vas occurs in up to 1% of men. Congenital unilateral absence of the vas deferens can be related to cystic fibrosis transmembrane conductance regulator mutations or in 79% of cases, renal agenesis. We present a case of each, diagnosed in children at operation for elective inguinal hernia repairs. One patient had associated ipsilateral renal agenesis with a normal cystic fibrosis screen. The other patient had an ipsilateral pelvic kidney and a mutation detected on cystic fibrosis screening. Current understanding of the embryology of the relationship between these defects would seem to be supported by our cases. Keywords: Absent vas, Cystic fibrosis, Renal agenesis, Embryologyhttp://www.sciencedirect.com/science/article/pii/S2214442013000363 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Gregory Shepherd Ashok Rajimwale |
spellingShingle |
Gregory Shepherd Ashok Rajimwale Embryology of the Absent Vas Supported by 2 Cases of Congenital Unilateral Absence of Vas With Varied Associations Urology Case Reports |
author_facet |
Gregory Shepherd Ashok Rajimwale |
author_sort |
Gregory Shepherd |
title |
Embryology of the Absent Vas Supported by 2 Cases of Congenital Unilateral Absence of Vas With Varied Associations |
title_short |
Embryology of the Absent Vas Supported by 2 Cases of Congenital Unilateral Absence of Vas With Varied Associations |
title_full |
Embryology of the Absent Vas Supported by 2 Cases of Congenital Unilateral Absence of Vas With Varied Associations |
title_fullStr |
Embryology of the Absent Vas Supported by 2 Cases of Congenital Unilateral Absence of Vas With Varied Associations |
title_full_unstemmed |
Embryology of the Absent Vas Supported by 2 Cases of Congenital Unilateral Absence of Vas With Varied Associations |
title_sort |
embryology of the absent vas supported by 2 cases of congenital unilateral absence of vas with varied associations |
publisher |
Elsevier |
series |
Urology Case Reports |
issn |
2214-4420 |
publishDate |
2014-03-01 |
description |
Congenital absence of the vas occurs in up to 1% of men. Congenital unilateral absence of the vas deferens can be related to cystic fibrosis transmembrane conductance regulator mutations or in 79% of cases, renal agenesis. We present a case of each, diagnosed in children at operation for elective inguinal hernia repairs. One patient had associated ipsilateral renal agenesis with a normal cystic fibrosis screen. The other patient had an ipsilateral pelvic kidney and a mutation detected on cystic fibrosis screening. Current understanding of the embryology of the relationship between these defects would seem to be supported by our cases. Keywords: Absent vas, Cystic fibrosis, Renal agenesis, Embryology |
url |
http://www.sciencedirect.com/science/article/pii/S2214442013000363 |
work_keys_str_mv |
AT gregoryshepherd embryologyoftheabsentvassupportedby2casesofcongenitalunilateralabsenceofvaswithvariedassociations AT ashokrajimwale embryologyoftheabsentvassupportedby2casesofcongenitalunilateralabsenceofvaswithvariedassociations |
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