Document Detail


Combined persistent Mullerian Duct Syndrome, Transverse Testicular Ectopia and Mosaic Klinefelter's Syndrome.
MedLine Citation:
PMID:  18760051     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Persistent Mullerian Duct Syndrome (PMDS), a rare form of male pseudohermaphroditism, is characterized by the persistence of Mullerian duct structures (uterus, fallopian tubes and upper two-thirds of vagina) in otherwise normallyvirilized males (Karyotype 46XY). Patients suffering from PMDS present with cryptorchidism, inguinal hernia and infertility. Diagnosis is established when Mullerian duct structures are discovered either during ultrasonography for localization of undescended testis(s), during surgical exploration for cryptorchidism or herniorrhaphy (hernii uteri inguinalis). Presence of both testes on one side of the scrotum is known as Transverse Testicular Ectopia (TTE). Co-existence of PMDS and transverse testicular ectopia in a patient of mosaic Klinefelter's syndrome (Karyotype 46XY/47XXY) is a unique genetic association.
Authors:
Abdul Rehman; Zubair Hasan; Samina Amanat; Tauseef Shaukat; Aisha Saeed; Kashif Jamil; Amjad Zaidi; M Akram
Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Journal of the College of Physicians and Surgeons--Pakistan : JCPSP     Volume:  18     ISSN:  1022-386X     ISO Abbreviation:  J Coll Physicians Surg Pak     Publication Date:  2008 Jun 
Date Detail:
Created Date:  2008-09-01     Completed Date:  2008-10-21     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9606447     Medline TA:  J Coll Physicians Surg Pak     Country:  Pakistan    
Other Details:
Languages:  eng     Pagination:  375-7     Citation Subset:  IM    
Affiliation:
Department of General Surgery, Pakistan Atomic Energy Commission Hospital, Islamabad. surgeonarehman@yahoo.com
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MeSH Terms
Descriptor/Qualifier:
Humans
Klinefelter Syndrome*
Male
Middle Aged
Mullerian Ducts / abnormalities*
Pseudohermaphroditism*
Syndrome
Testis / abnormalities*

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


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