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10.1590/S1677-5538.IBJU.2016.0225

http://scihub22266oqcxt.onion/10.1590/S1677-5538.IBJU.2016.0225
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C5117982!5117982 !27532119
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suck abstract from ncbi


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pmid27532119
      Int+Braz+J+Urol 2016 ; 42 (6 ): 1237-1243
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  • Persistent Mullerian Duct Syndrome: a rare entity with a rare presentation in need of multidisciplinary management #MMPMID27532119
  • Da Aw L ; Zain MM ; Esteves SC ; Humaidan P
  • Int Braz J Urol 2016[Nov]; 42 (6 ): 1237-1243 PMID27532119 show ga
  • 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 multidisciplinar 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.
  • |Abdomen/diagnostic imaging [MESH]
  • |Adolescent [MESH]
  • |Disorder of Sex Development, 46,XY/*diagnosis/diagnostic imaging [MESH]
  • |Disorders of Sex Development/*diagnosis/diagnostic imaging [MESH]
  • |Female [MESH]
  • |Humans [MESH]
  • |Hydrocolpos/*diagnosis/diagnostic imaging [MESH]
  • |Male [MESH]


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