Results 101 to 110 of about 1,042 (196)

Herlyn–Werner–Wünderlich syndrome: An unusual case with presentation of menorrhagia

open access: yesTaiwanese Journal of Obstetrics & Gynecology, 2020
Objective: Herlyn–Werner–Wünderlich (HWW) syndrome is a rare condition in which patients present with a palpable pelvic mass and pain caused by an obstructed hemivagina. Here we present a case of HWW syndrome characterized by prolonged menstrual bleeding.
Hsin-I Liang   +3 more
doaj   +1 more source

UTERUS DIDELPHYS IN NULLIPAROUS AND MULTIPAROUS WOMEN – A RARE ENTITY [PDF]

open access: yes, 2021
Uterus didelphys is a rare congenital uterine abnormality in which the embryogenetic fusion of the Mullerian ducts fails to occur. It will lead to the formation of a double uterus with two separate cervices and most often a double vagina with a ...
CHOUREY, NIRAJ   +5 more
core   +1 more source

Herlyn-Weber-Wunderlich syndrome with ectopic ureter in prepubertal female

open access: yesJournal of Indian Association of Pediatric Surgeons, 2014
We report a rare case of uterovaginal duplication in a prepubertal female. The patient also had a permeable ureter (ureter with urine passing through it) subtending a poorly functioning kidney with ectopic insertion in the obstructed hemivagina.
Saurabh Garge   +9 more
doaj   +1 more source

Giant colpolithiasis in urogenital sinus anomaly with urethral duplication: A case report and review of literature

open access: yesAfrican Journal of Paediatric Surgery
Primary vaginal calculi are uncommon in children. Urethral duplication in females is seen to occur in association with complex congenital malformations. We report the case of perianal persistent urogenital sinus with a hypertrophied clitoris with phallic
Shreyas Dudhani   +4 more
doaj   +1 more source

An unusual appearance of the post-pubertal Herlyn-Werner-Wunderlich syndrome with acute abdominal pain: A case report [PDF]

open access: yes, 2019
Background: Herlyn-Werner-Wunderlich (HWW) syndrome is a rare congenital urogenital defect. It is detected by unilateral low vaginal obstruction, uterus didelphys, and ipsilateral kidney agenesis.
Esmailzadeh, Arezoo, Ghasemi, Marzieh
core   +3 more sources

An interesting case of Herlyn–Werner–Wunderlich syndrome

open access: yesTzu Chi Medical Journal, 2020
Herlyn–Werner–Wunderlich syndrome (HWWS) is a rare congenital anomaly characterized by uterus didelphys with blind hemivagina and ipsilateral renal agenesis.
Maureen P Tigga
doaj   +1 more source

Uterus didelphys with unilateral obstructed hemivagina with hematometrocolpos and hematosalpinx with ipsilateral renal agenesis

open access: yesJournal of Human Reproductive Sciences, 2009
Uterus didelphys with blind hemivagina and ipsilateral renal agenesis (Herlyn Werner-Wunderlich Syndrome) is a rare congenital anomaly. It mostly presents with severe dysmenorrhea and a palpable mass due to unilateral hematocolpos.
Gaurav Jindal   +3 more
doaj   +1 more source

A rare case presentation of an anomalous uterus mimicking ovarian tumour [PDF]

open access: yes, 2017
Mullerian anomalies occur in 1:1000-3000 females. Uterus didelphys and obstructed hemangioma with a septum contribute to 10% anomalies. Young girls present with severe dysmenorrhea, hematometra, hematocolpos and recurrent pregnancy loss.
M., Mohanambal, sheelaa, Wills G.
core   +2 more sources

OHVIRA syndrome and its incomplete variant: multimodality imaging insights from two distinct presentations of Müllerian-renal anomalies [PDF]

open access: yes
Mullerian anomalies such as obstructed hemivagina and ipsilateral renal anomaly (OHVIRA) syndrome pose diagnostic challenges due to their embryological variability and diverse clinical presentations.
B. S., Pavan, Pavuluri, Viharika
core   +2 more sources

A rare case report of urogenital anomaly in a teenage girl: Herlyn–Werner–Wunderlich syndrome/OHVIRA syndrome (Obstructed Hemivagina and Ipsilateral Renal Anomaly)

open access: yesThe Egyptian Journal of Radiology and Nuclear Medicine
Background Herlyn–Werner–Wunderlich syndrome also known as OHVIRA syndrome is a rare complex congenital developmental anomaly characterized by the triad of uterine didelphys, obstructed hemivagina causing hematometrocolpos and ipsilateral renal anomaly ...
Govardhana Das Joel   +2 more
doaj   +1 more source

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