Literature DB >> 20859029

Persistent Mullerian duct syndrome: a case report and review of the literature.

Temitope O Odi1, Lukman O Abdur-Rahman, Abdulrasheed A Nasir.   

Abstract

Persistent Mullerian duct syndrome is a rare form of internal male pseudohermaphroditism, in which Mullerian duct derivatives (uterus and fallopian tubes) are present in a genotypic (46XY) and phenotypic male. Over 150 cases have been reported, mainly from outside the African setting. This article presents an unexpected case encountered in an African setting. Handicaps in the management were unavailability of necessary diagnostic tools as well as lack of finance to assess those available. Although a diagnosis was eventually arrived at and the parents thoroughly counseled, the patient has not represented for definitive surgery.

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Year:  2010        PMID: 20859029     DOI: 10.4103/0189-6725.70425

Source DB:  PubMed          Journal:  Afr J Paediatr Surg        ISSN: 0974-5998


  6 in total

1.  Indirect inguinal hernia with uterine tissue in a male: A case of persistent Mullerian duct syndrome and literature review.

Authors:  Michael Ahdoot; Motaz Qadan; Monica Santa-Maria; William A Kennedy; Aaron Ilano
Journal:  Can Urol Assoc J       Date:  2013 Jan-Feb       Impact factor: 1.862

2.  Persistent mullerian duct syndrome with transverse testicular ectopia: rare entity.

Authors:  Abhay Kumar
Journal:  J Clin Diagn Res       Date:  2014-03-15

3.  Persistent Mullerian Duct Syndrome with Ovarian Endometriosis-A Rare Case Report.

Authors:  Savitri Mallikarjun Nerune; Surekha B Hippargi; Namrata B Mestri; Nikhil M Mehrotra
Journal:  J Clin Diagn Res       Date:  2016-02-01

4.  Persistent Müllerian duct syndrome: A case report and review.

Authors:  Xiaoya Ren; Di Wu; Chunxiu Gong
Journal:  Exp Ther Med       Date:  2017-10-11       Impact factor: 2.447

5.  Novel homozygous mutation in a colombian patient with persistent müllerian duct syndrome: expanded phenotype.

Authors:  Mary García Acero; Olga Moreno; Andrés Gutiérrez; Catalina Sánchez; Juan Guillermo Cataño; Fernando Suárez-Obando; Adriana Rojas
Journal:  Int Braz J Urol       Date:  2019 Sep-Oct       Impact factor: 3.050

6.  Genome-wide association study identifies common and low-frequency variants at the AMH gene locus that strongly predict serum AMH levels in males.

Authors:  John R B Perry; George McMahon; Felix R Day; Susan M Ring; Scott M Nelson; Debbie A Lawlor
Journal:  Hum Mol Genet       Date:  2015-11-24       Impact factor: 6.150

  6 in total

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