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Information Journal Paper

Title

HERLYN WERNER WUNDERLICH SYNDROME WITH HEMATOCOLPOS: AN UNUSUAL CASE REPORT OF FULL DIAGNOSTIC APPROACH AND TREATMENT (CASE REPORT)

Pages

  136-140

Abstract

 Herlyn-Werner-Wunderlich (HWW) syndrome is an uncommon combined mullerian duct anomalies (MDAs) and mesonephric duct malformation of female urogenital tract characterized by uterus didelphys and obstructed hemi-vagina and ipsilateral renal agenesis (OHVIRA) syndrome. We present a rare and unusual case of this syndrome in a 19 year-old female who suffered from hypomenorrhoea and abdominal pain. She had an obstructed hemi-vagina on right side which led to marked distention of ipsilateral cervix, while proximal hemi-vagina compressed the contralateral side causing its partial obstruction resulting in hypomenorrhoea. Understanding the imaging findings of this rare condition is important for early diagnosis in order to prevent complications which may lead to INFERTILITY.

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    APA: Copy

    BHOIL, ROHIT, AHLUWALIA, AJAY, & CHAUHAN, NARVIR. (2016). HERLYN WERNER WUNDERLICH SYNDROME WITH HEMATOCOLPOS: AN UNUSUAL CASE REPORT OF FULL DIAGNOSTIC APPROACH AND TREATMENT (CASE REPORT). INTERNATIONAL JOURNAL OF FERTILITY AND STERILITY, 10(1), 136-140. SID. https://sid.ir/paper/305868/en

    Vancouver: Copy

    BHOIL ROHIT, AHLUWALIA AJAY, CHAUHAN NARVIR. HERLYN WERNER WUNDERLICH SYNDROME WITH HEMATOCOLPOS: AN UNUSUAL CASE REPORT OF FULL DIAGNOSTIC APPROACH AND TREATMENT (CASE REPORT). INTERNATIONAL JOURNAL OF FERTILITY AND STERILITY[Internet]. 2016;10(1):136-140. Available from: https://sid.ir/paper/305868/en

    IEEE: Copy

    ROHIT BHOIL, AJAY AHLUWALIA, and NARVIR CHAUHAN, “HERLYN WERNER WUNDERLICH SYNDROME WITH HEMATOCOLPOS: AN UNUSUAL CASE REPORT OF FULL DIAGNOSTIC APPROACH AND TREATMENT (CASE REPORT),” INTERNATIONAL JOURNAL OF FERTILITY AND STERILITY, vol. 10, no. 1, pp. 136–140, 2016, [Online]. Available: https://sid.ir/paper/305868/en

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