{"paper_id":"1049fc2c-58f4-4183-9af6-894f9ed76a1b","body_text":"Herlyn-Werner-Wunderlich syndrome: case reports\n| Author |\n|---|\n| Date | Start Page | End Page |\n|---|---|---|\n2025-03-19 | 1 | 1 |\nHerlyn-Werner-Wunderlich (HWW) syndrome is a rare congenital Müllerian anomaly characterized by uterus didelphys, obstructed hemivagina, and ipsilateral renal agenesis. It typically presents during adolescence with dysmenorrhea, pelvic pain, and, in some cases, a palpable pelvic mass due to hematocolpos or hematometra. Early diagnosis is crucial to prevent complications such as endometriosis and infertility. Imaging techniques, particularly MRI and ultrasound, play a key role in detection. Treatment involves surgical correction, usually through vaginal septum resection, to restore normal menstrual flow and alleviate symptoms. Multidisciplinary management is recommended for optimal patient outcomes. A clinical case of HWW syndrome in 13 year old girl will be presented.","source_license":"CC0","license_restricted":false}