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10.1590/S1677-5538.IBJU.2016.0225 http://scihub22266oqcxt.onion/10.1590/S1677-5538.IBJU.2016.0225 C5117982!5117982!27532119     free     free     free Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 245.2 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Int+Braz+J+Urol 2016 ; 42 (6): 1237-43 Nephropedia Template TP {{tp|p=27532119|t=2016. Persistent Mullerian Duct Syndrome: a rare entity with a rare presentation in need of multidisciplinary management |pdf=|usr=}}{{27532119}} gab.com Text Persistent Mullerian Duct Syndrome: a rare entity with a rare presentation in need of multidisciplinary management JO: Int Braz J Urol http://www.kidney.de/pget.php?&tw=1&pmid=27532119 #FOAvip Main findings:: A typical male looking adolescent with a legal female gender assignment presented with haematuria. Investigations led to the diagnosis of Persistent Mullerian Duct Syndrome. The condition is indeed a rare entity that needs a multidisciplinary team management. Case hypothesis:: A case of Persistent Mullerian Duct Syndrome undiagnosed at birth because karyotyping was defaulted, thus resulting in a significant impact on the legal gender assignment and psychosocial aspects. Promising future implications:: The reporting of this case is important to create awareness due to its rarity coupled with the rare presentation with hematuria as a possible masquerade to menstruation. There were not only medical implications, but also psychosocial and legal connotations requiring a holistic multidisciplinary management. Twit Text FOAVip Persistent Mullerian Duct Syndrome: a rare entity with a rare presentation in need of multidisciplinary management ????Int Braz J Urol http://www.kidney.de/pget.php?&tw=1&pmid=27532119 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27532119 #FOAvip English Wikipedia <ref>{{Cite pmid|27532119}}</ref> Persistent Mullerian Duct Syndrome: a rare entity with a rare presentation in need of multidisciplinary management #MMPMID27532119 Aw LD; Zain MM; Esteves SC; Humaidan P Int Braz J Urol 2016[Nov]; 42 (6): 1237-43 PMID27532119show ga Main findings:: A typical male looking adolescent with a legal female gender assignment presented with haematuria. Investigations led to the diagnosis of Persistent Mullerian Duct Syndrome. The condition is indeed a rare entity that needs a multidisciplinary team management. Case hypothesis:: A case of Persistent Mullerian Duct Syndrome undiagnosed at birth because karyotyping was defaulted, thus resulting in a significant impact on the legal gender assignment and psychosocial aspects. Promising future implications:: The reporting of this case is important to create awareness due to its rarity coupled with the rare presentation with hematuria as a possible masquerade to menstruation. There were not only medical implications, but also psychosocial and legal connotations requiring a holistic multidisciplinary management. äPersistent Mullerian Duct Syndrome: a rare entity with a rare presenta(epmc).pdf DeepDyve Pubget Overpricing