Literature DB >> 9297443

Further arguments for non-fortuitous association of Potter sequence with XYY males.

S Rudnik-Schöneborn1, H M Schüler, G Schwanitz, M Hansmann, K Zerres.   

Abstract

Although large studies on sex chromosome abnormalities have not detected a higher incidence of malformations in 47,XYY males, several case reports suggest that there is an association between renal agenesis or cystic dysplasia of the kidney and XYY status. The authors report 3 further infants with XYY karyotype who had urogenital malformations leading to Potter sequence. On the basis of our observations and review of the literature, we suggest that the XYY syndrome and Potter sequence are more significantly associated than expected by pure coincidence.

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Year:  1996        PMID: 9297443

Source DB:  PubMed          Journal:  Ann Genet        ISSN: 0003-3995


  2 in total

1.  Copy-number variation associated with congenital anomalies of the kidney and urinary tract.

Authors:  Georgina Caruana; Milagros N Wong; Amanda Walker; Yves Heloury; Nathalie Webb; Lilian Johnstone; Paul A James; Trent Burgess; John F Bertram
Journal:  Pediatr Nephrol       Date:  2014-10-01       Impact factor: 3.714

2.  Embryo with XYY syndrome presenting with clubfoot: a case report.

Authors:  Dimitrios Athanatos; Christos Tsakalidis; George P Tampakoudis; Maria N Papastergiou; Fillipos Tzevelekis; George Pados; Efstratios A Assimakopoulos
Journal:  Cases J       Date:  2009-09-01
  2 in total

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