Literature DB >> 2359010

Persistent Mullerian duct syndrome: report of two boys with associated crossed testicular ectopia.

E S Mahfouz1, M A Issa, T I Farag, K K Naguib, S A al-Awadi, R N Schimke.   

Abstract

Persistent Mullerian duct structures and crossed testicular ectopia were found in two phenotypically normal, unrelated males, with 46,XY karyotype, during routine herniorrhaphy. In each case, the vascular supply to the ectopic testis originated from the appropriate ipsilateral side. The clinical significance and genetic implications of this rare association are discussed.

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Year:  1990        PMID: 2359010     DOI: 10.1016/0022-3468(90)90367-i

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN: 0022-3468            Impact factor:   2.545


  2 in total

1.  [Persistent mullerian duct syndrome : Rare incidental finding during treatment of pediatric inguinal hernia].

Authors:  P Sperling; T Meyer
Journal:  Urologe A       Date:  2017-04       Impact factor: 0.639

Review 2.  Misdiagnosed transverse testicular ectopia: a rare entity.

Authors:  A Pandey; D K Gupta; A N Gangopadhyay; S P Sharma
Journal:  Hernia       Date:  2008-10-03       Impact factor: 4.739

  2 in total

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