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<article xlink="http://www.w3.org/1999/xlink" dtd-version="1.0" article-type="healthcare" lang="en"><front><journal-meta><journal-id journal-id-type="publisher">IJCRR</journal-id><journal-id journal-id-type="nlm-ta">I Journ Cur Res Re</journal-id><journal-title-group><journal-title>International Journal of Current Research and Review</journal-title><abbrev-journal-title abbrev-type="pubmed">I Journ Cur Res Re</abbrev-journal-title></journal-title-group><issn pub-type="ppub">2231-2196</issn><issn pub-type="opub">0975-5241</issn><publisher><publisher-name>Radiance Research Academy</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">361</article-id><article-id pub-id-type="doi"/><article-id pub-id-type="doi-url"/><article-categories><subj-group subj-group-type="heading"><subject>Healthcare</subject></subj-group></article-categories><title-group><article-title>A RARE CASE OF PERSISTENT MULLERIAN DUCT SYNDROME PRESENTING AS HERNIA UTERO INGUINALIS&#13;
</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Murugesan</surname><given-names>N.</given-names></name></contrib><contrib contrib-type="author"><name><surname>Viswanathan</surname><given-names>M. S.</given-names></name></contrib><contrib contrib-type="author"><name><surname>S.</surname><given-names>Lakshmanan</given-names></name></contrib><contrib contrib-type="author"><name><surname>Surana</surname><given-names>Pankaj</given-names></name></contrib><contrib contrib-type="author"><name><surname>Anbhazakan</surname><given-names>R.</given-names></name></contrib></contrib-group><volume/><issue/><fpage>16</fpage><lpage>19</lpage><permissions><copyright-statement>This article is copyright of Popeye Publishing, 2009</copyright-statement><copyright-year>2009</copyright-year><license license-type="open-access" href="http://creativecommons.org/licenses/by/4.0/"><license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution (CC BY 4.0) Licence. You may share and adapt the material, but must give appropriate credit to the source, provide a link to the licence, and indicate if changes were made.</license-p></license></permissions><abstract><p>The aim of presentation of this rare case of persistent mullerian duct syndrome is to outline management of such case when encountered unexpectedly while operating on obstructed inguinal hernia. More so this possibility should be kept in mind while operating on a case of cryptorchidism. PMDS is a rare condition often missed in a casual USG done in emergency this leads to confusion to surgeon while operating. Left behind gonads pose a risk of malignant degeneration if ignored and hence will need further management. Presence of risk of infertility after definitive treatment especially in young patients precludes immediate surgical removal of gonads in such patients. Proper informed consent prior to such procedure is important as is advise on future fertility.&#13;
</p></abstract><kwd-group><kwd>Persistent mullerian duct syndrome (PMDS)</kwd><kwd> Pseudohermaphroditism</kwd><kwd> Transverse testicular ectopia (TTE)</kwd><kwd> Cryptorchidism</kwd><kwd> Hernia utero inguinalis</kwd></kwd-group></article-meta></front></article>
