Literature DB >> 18177653

Congenital radioulnar synostosis, azoospermia, and pseudodicentric Y chromosome.

Akheel A Syed1, Richard Quinton.   

Abstract

Congenital radioulnar synostosis is a rare skeletal defect associated with certain chromosomal abnormalities. We describe the first report of its occurrence in association with a pseudodicentric Y chromosome in a 27-year-old man with azoospermia and testicular dysfunction.

Entities:  

Mesh:

Year:  2008        PMID: 18177653     DOI: 10.1016/j.fertnstert.2007.09.059

Source DB:  PubMed          Journal:  Fertil Steril        ISSN: 0015-0282            Impact factor:   7.329


  2 in total

1.  The developmental spectrum of proximal radioulnar synostosis.

Authors:  Alison M Elliott; Lisa Kibria; Martin H Reed
Journal:  Skeletal Radiol       Date:  2010-01       Impact factor: 2.199

2.  Congenital radioulnar synostosis - case report.

Authors:  Anna Siemianowicz; Wojciech Wawrzynek; Krzysztof Besler
Journal:  Pol J Radiol       Date:  2010-10
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.