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Herlyn-Werner-Wunderlich Syndrome: A Case Report [PDF]

open access: yesJournal of Nepal Medical Association, 2023
Herlyn-Werner-Wunderlich syndrome is a rare Mullerian and mesonephric ductal anomaly characterized by a triad of didelphys uterus, obstructed hemivagina, and ipsilateral renal agenesis complex.
Priyanka Vaidya   +2 more
doaj   +9 more sources

Herlyn Werner Wunderlich Syndrome with Hematocolpos Symptom. [PDF]

open access: yesOpen Access Maced J Med Sci, 2019
BACKGROUND: Uterodidelphys with obstructed hemivagina and ipsilateral renal agenesis is referred to as the Herlyn Werner Wunderlich (HWW) syndrome. Herlyn-Werner-Wunderlich (HWW) syndrome is a very rare congenital anomaly of the urogenital tract involving Müllerian ducts and Wolffian structures, and it is Werner by the triad of uterus didelphys ...
Rusda M, Umara A, Rambe AYM.
europepmc   +7 more sources

Herlyn–Werner–Wunderlich syndrome

open access: yesMedical Journal of Dr. D.Y. Patil University, 2017
Herlyn–Werner–Wunderlich syndrome is a rare developmental anomaly, in which there is uterus didelphys with obstructed hemivagina and ipsilateral renal agenesis.
Himadri Bal   +3 more
doaj   +5 more sources

Uterus Didelphys with Hematocervix in the Unilateral Obstructed Hemivagina and Ipsilateral Renal Agenesis: A Case Report of Herlyn–Werner–Wunderlich Syndrome [PDF]

open access: yesReproductive Medicine
Background: Mullerian duct anomalies include a broad spectrum of genital tract defects that arise from developmental abnormalities of the genital tract.
Cristina Taliento   +6 more
doaj   +6 more sources

Herlyn-Werner-Wunderlich syndrome: A case report in a young woman, with literature review [PDF]

open access: yesRadiology Case Reports, 2022
Herlyn-Werner-Wunderlich syndrome is a rare complex congenital disorder, with combined Müllerian and mesonephric duct anomalies, presenting with uterus didelphys, unilateral blind hemivagina and ipsilateral renal agenesis. Hemivaginal obstruction usually
Eduardo Negrão, MD   +4 more
doaj   +2 more sources

Herlyn-Werner-Wunderlich syndrome: A report of three cases in adolescents and adult woman [PDF]

open access: yesRadiology Case Reports, 2021
We report three cases with Herlyn-Werner-Wunderlich syndrome in adolescents and young female. The objective of this report was to describe the clinical presentation, ultrasound (US) and magnetic resonance imaging (MRI) findings of Herlyn-Werner ...
Quynh Vo Nhu, MD   +2 more
doaj   +2 more sources

Herlyn-Werner-Wunderlich (HWW) Syndrome

open access: yesApollo Medicine, 2016
Obstructed hemivagina and ipsilateral renal anomaly (OHVIRA), also known as Herlyn–Werner–Wunderlich syndrome, is a rare syndrome constituting  0.16–3% of all the mullerian duct anomalies. Patients are symptomatic shortly after menarche when hematocolpos develop during menstruation, resulting in dysmenorrhea and a pelvic mass.
U. Nagashree, D. Vasanthi
doaj   +4 more sources

Herlyn Werner Wunderlich Syndrome with Hydrocolpos: A Case Report [PDF]

open access: yesJournal of Nepal Medical Association
Herlyn-Werner-Wunderlich Syndrome is a very rare congenital malformation of the urogenital tract involving both the Mullerian and Wolffian ducts characterized by the triad uterine diadelphys, obstructed vagina, and unilateral renal agenesis.
Saurav Sen Oli   +4 more
doaj   +2 more sources

Herlyn-Werner-Wunderlich syndrome in a adolescent girl [PDF]

open access: yesLiječnički vjesnik, 2023
Herlyn-WernerWunderlich syndrome (HWWS) is a rare congenital genitourinary anomaly with uterine anomalies, unilateral cervicovaginal obstruction, and ipsilateral renal anomalies resulting from the embryological arrest of Müllerian and mesonephric ducts ...
Vita Jugovac   +4 more
doaj   +2 more sources

Herlyn-Werner-Wunderlich syndrome with borderline serous cystadenoma of the ovary: case report and literature review [PDF]

open access: yesRadiology Case Reports, 2021
Herlyn-Werner-Wunderlich syndrome, is a rare urogenital congenital anomaly. Coexisting Mullerian ducts anomalies and ovarian neoplasms are rarely reported.
Johara AlMulhim, MD   +1 more
doaj   +2 more sources

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