Results 61 to 70 of about 1,327 (186)

OHVIRA syndrome: a rare variant of mullerian duct anomaly [PDF]

open access: yes, 2016
OHVIRA is a rare variety of congenital anomaly of mullerian duct. The syndrome includes uterus didelphys, obstructed hemivagina and ipsilateral renal anomaly, also known as Herlyn-Werner-Wunderlich (HWW) syndrome.
Dahiya, Nidhi, Rudra, Samar
core   +2 more sources

Herlyn-Werner-Wunderlich syndrome presenting with dysmenorrhea: a case report

open access: yesJournal of Medical Case Reports, 2019
Background Herlyn-Werner-Wunderlich syndrome is a rare congenital anomaly characterized by uterus didelphys, obstructed hemivagina, and ipsilateral renal agenesis. The most common presentation is abdominal pain, dysmenorrhea, and abdominal mass secondary
Dilruba Sharmen Nishu   +5 more
doaj   +1 more source

A Rare Obstetric Outcome in Uterus Didelphys with Obstructed Hemivagina and Ipsilateral Renal Agenesis [PDF]

open access: yes, 2012
Background: The unique clinical syndrome of uterus didelphys, obstructed hemivagina, and ipsilateral renal anomaly is very rare and can be quite difficult to recognize because of the enormous heterogeneity in its clinical presentation.
Francisco, C   +3 more
core   +1 more source

Diagnosis and Treatment in a Tertiary Hospital of a Series of Complex Genital Malformations Corresponding to Double Uterus with Obstructed Hemivagina and Ipsilateral Renal Agenesis

open access: yesInternational Journal of Reproductive Medicine, Volume 2018, Issue 1, 2018., 2018
Aim. To evaluate the clinical features, diagnostic routine, treatment, and prognosis of patients with double uterus with obstructed hemivagina and ipsilateral renal agenesis at a University Hospital. Methods. A retrospective study analyzing the medical charts of outpatients with similar complex genital malformations seen at the University Hospital of ...
Júlia Kefalás Troncon   +6 more
wiley   +1 more source

An Unexpected Cause of Pelvic Pain in a Pubertal Case: Herlyn-Werner-Wunderlich Syndrome

open access: yesHaseki Tıp Bülteni, 2014
Uterovaginal duplication with imperforated hemivagina is a rare type of Mullerian anomaly. If ipsilateral renal agenesis is associated with this complex genital malformation, it is called Herlyn-Werner-Wunderlich syndrome.
Yasemin Kayadibi   +4 more
doaj   +1 more source

Herlyn-Werner-Wunderlich syndrome: a case report [PDF]

open access: yesRevista Brasileira de Ginecologia e Obstetrícia, 2015
Herlyn-Werner-Wunderlich (HWW) syndrome is a rare congenital disorder of the Müllerian ducts in which there is uterus didelphys, obstructed hemivagina and unilateral renal agenesis.
Pedro Salomao Piccinini, John Doski
doaj   +2 more sources

Herlyn–Werner–Wunderlich Syndrome: Presentation and Surgical Management Options for Five Cases [PDF]

open access: yes, 2015
Background: Herlyn?Werner?Wunderlich syndrome is a rare Müllerian-duct anomaly consisting of uterine didelphys, a unilateral obstructed hemivagina, and ipsilateral renal agenesis.
Abuzeid, Mostafa I.   +4 more
core   +1 more source

Didelphys Uterus: A Case Report and Review of the Literature

open access: yesCase Reports in Obstetrics and Gynecology, Volume 2015, Issue 1, 2015., 2015
Background. Mullerian duct anomalies (MDAs) are congenital defects of the female genital system that arise from abnormal embryological development of the Mullerian ducts. A didelphys uterus, also known as a “double uterus,” is one of the least common amongst MDAs. This report discusses a case of didelphys uterus that successfully conceived, carried her
Shadi Rezai   +6 more
wiley   +1 more source

The Herlyn-Werner-Wunderlich (HWW) syndrome– A rare case report [PDF]

open access: yes, 2023
A 20-year-old unmarried female, student by occupation, well built and nourished presented with intermenstrual spotting from past 1 month. No h/o pelvic pain/ mass/ fever. No h/o of similar complaints in the past. Attained menarche at 14 years.
H L, Dr Harisha, Dr   +2 more
core   +1 more source

Rupture of Didelphys Uterus and Coexistence of Intestinal Diverticulum in an 18 Years Old Primigravida: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 1, January 2026.
ABSTRACT Uterine didelphys, also known as double uterus, is a congenital anomaly of the female reproductive system that can be associated with a significant number of threatening obstetric complications, such as uterine rupture. We report a rare and complex case of an 18‐year‐old primigravida who presented with uterine rupture due to uterine didelphys ...
Asim Ali   +7 more
wiley   +1 more source

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