TY - CHAP M1 - Book, Section TI - Herlyn-Werner-Wunderlich Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - It is a rare genetic disorder characterized by the presence of a uterus didelphys, a blind hemivagina and ipsilateral renal agenesis. Individuals affected may have either completely or incompletely obstructed vaginal septum. The most common presentation is acute or progressive lower abdominal pain, dysmenorrhea (especially in Type I), and abdominal mass in the lower abdomen secondary to hematocolpos and/or hematometra. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/29 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164072904 ER -