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10.4111/icu.2016.57.5.367 http://scihub22266oqcxt.onion/10.4111/icu.2016.57.5.367 C5017564!5017564 !27617320     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=27617320 &cmd=llinks): Failed to open stream: HTTP request failed! 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An unusual cause of urinary incontinence: Urethral coitus in a case of Mayer-Rokitansky-Kuster-Hauser syndrome |pdf=|usr=}}{{27617320 }} gab.com Text An unusual cause of urinary incontinence: Urethral coitus in a case of Mayer-Rokitansky-Kuster-Hauser syndrome JO: Investig Clin Urol http://www.kidney.de/pget.php?&tw=1&pmid=27617320 #FOAvip Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a rare anomaly in women and is characterized by congenital aplasia of the uterus and vagina, with normal development of secondary sexual characteristics and a normal karyotype. We report a case of a 38-year-old women with MRKH syndrome that had experienced urethral sex for many years. She presented with urinary incontinence and dyspareunia. The patient's secondary sexual characteristics were normal, and examination revealed a widely open incompetent megalourethra and an absent vagina. Laboratory studies confirmed a 46, XX karyotype. Imaging included ultrasonography and magnetic resonance imaging, which indicated bilateral normal ovaries and a rudimental bicornuate uterus. After confirming the diagnosis of MRKH, the patient underwent urethroplasty by urethral plication, antiincontinence surgery by autologous fascial sling of the bladder neck, and the creation of a neo-vagina using a urethral flap. After 3 months, voiding cystourethrography and uroflowmetry confirmed normal voiding. There were no postoperative symptoms of urinary incontinence, and the patient was completely satisfied. Twit Text FOAVip An unusual cause of urinary incontinence: Urethral coitus in a case of Mayer-Rokitansky-Kuster-Hauser syndrome ????Investig Clin Urol http://www.kidney.de/pget.php?&tw=1&pmid=27617320 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27617320 #FOAvip English Wikipedia <ref>{{Cite pmid|27617320 }}</ref> An unusual cause of urinary incontinence: Urethral coitus in a case of Mayer-Rokitansky-Kuster-Hauser syndrome #MMPMID27617320 Sharifiaghdas F ; Daneshpajooh A ; Sohbati S ; Mirzaei M Investig Clin Urol 2016[Sep]; 57 (5 ): 367-71 PMID27617320 show ga Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a rare anomaly in women and is characterized by congenital aplasia of the uterus and vagina, with normal development of secondary sexual characteristics and a normal karyotype. We report a case of a 38-year-old women with MRKH syndrome that had experienced urethral sex for many years. She presented with urinary incontinence and dyspareunia. The patient's secondary sexual characteristics were normal, and examination revealed a widely open incompetent megalourethra and an absent vagina. Laboratory studies confirmed a 46, XX karyotype. Imaging included ultrasonography and magnetic resonance imaging, which indicated bilateral normal ovaries and a rudimental bicornuate uterus. After confirming the diagnosis of MRKH, the patient underwent urethroplasty by urethral plication, antiincontinence surgery by autologous fascial sling of the bladder neck, and the creation of a neo-vagina using a urethral flap. After 3 months, voiding cystourethrography and uroflowmetry confirmed normal voiding. There were no postoperative symptoms of urinary incontinence, and the patient was completely satisfied. |*Coitus [MESH] |46, XX Disorders of Sex Development/*complications/surgery [MESH] |Adult [MESH] |Congenital Abnormalities/surgery [MESH] |Female [MESH] |Humans [MESH] |Mullerian Ducts/*abnormalities/surgery [MESH] |Suburethral Slings [MESH] |Surgically-Created Structures [MESH] |Syndrome [MESH] |Urethra/abnormalities/surgery [MESH]An unusual cause of urinary incontinence: Urethral coitus in a case of(epmc).pdf DeepDyve Pubget Overpricing