Document Detail


Persistent Mullerian duct syndrome: a case report and review of the literature.
MedLine Citation:
PMID:  20859029     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
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.
Authors:
Temitope O Odi; Lukman O Abdur-Rahman; Abdulrasheed A Nasir
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Publication Detail:
Type:  Case Reports; Journal Article; Review    
Journal Detail:
Title:  African journal of paediatric surgery : AJPS     Volume:  7     ISSN:  0974-5998     ISO Abbreviation:  Afr J Paediatr Surg     Publication Date:    2010 Sep-Dec
Date Detail:
Created Date:  2010-09-22     Completed Date:  2010-10-26     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  101255062     Medline TA:  Afr J Paediatr Surg     Country:  Nigeria    
Other Details:
Languages:  eng     Pagination:  191-3     Citation Subset:  IM    
Affiliation:
Department of Surgery, University of Ilorin Teaching Hospital, Ilorin, Nigeria. oditemi@yahoo.com
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MeSH Terms
Descriptor/Qualifier:
Child, Preschool
Hernia, Inguinal / etiology
Humans
Male
Mullerian Ducts / abnormalities*
Pseudohermaphroditism / complications,  diagnosis*
Syndrome

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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