Abstract
IntroductionDidelphys uterus, or “double uterus,” is one of the rarest Müllerian duct anomalies (MDA). Due to its rarity, data are sparse on overall outcomes associated with this congenital defect, but it may be associated with several complications, both pregnancy and non-pregnancy related.Case ReportIn this case, a pregnant 35-year-old female with vaginal bleeding was subsequently diagnosed with uterus didelphys by transvaginal ultrasound imaging.ConclusionDespite its rarity, clinicians should be aware of MDAs and their associated compli-cations with pregnancy.
Highlights
Didelphys uterus, or “double uterus,” is one of the rarest Müllerian duct anomalies (MDA)
Despite its rarity, clinicians should be aware of MDAs and their associated complications with pregnancy. [Clin Pract Cases Emerg Med. 2021;5(4):447-449.]
It is characterized with Herlyn-Werner-Wunderlich syndrome, a rare disorder associated with obstructed hemivagina and ipsilateral renal agenesis
Summary
“double uterus,” is one of the rarest Müllerian duct anomalies (MDA). Case Report: In this case, a pregnant 35-year-old female with vaginal bleeding was subsequently diagnosed with uterus didelphys by transvaginal ultrasound imaging
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