Results 71 to 80 of about 1,436 (213)

Endometrial imaging [PDF]

open access: yes, 2012
The endometrium demonstrates a wide spectrum of normal and pathologic appearances throughout menarche as well as during the prepubertal and postmenopausal years and the first trimester of pregnancy. Characteristic morphologic changes take place in
Vassallo, Pierre
core  

Conservative treatment of Herlyn-Werner-Wunderlich syndrome: Analysis and long-term follow-up of 51 cases [PDF]

open access: yes, 2022
Objective: The purpose of this study is to analyze the precise anatomical characteristics of a large group of patients with Herlyn-Werner-Wunderlich syndrome together with the long-term follow-up and the reproductive performance.
Candiani, M   +5 more
core   +1 more source

Expansion of the core features of VACTERL association to include genital anomalies

open access: yesAmerican Journal of Medical Genetics Part A, Volume 194, Issue 9, September 2024.
Abstract Genital anomalies have been reported with VACTERL association but not considered a core feature. Acute and chronic complications stemming from unrecognized genital anomalies have been reported in adolescents and young adults with VACTERL association. We sought to determine the frequency and severity of genital anomalies in VACTERL patients and
Laura T. Forero   +4 more
wiley   +1 more source

Management of Transverse Septum in A Low Resource Setting-A Case Report Study

open access: yesPAMJ Clinical Medicine, 2020
Transverse vaginal septum is a rare female genital tract anomaly which may occur exclusive of any concomitant anomalies. We report the case of a pre menercheal girl who presented at our resource constrained center with primary amenorrhoea and cyclic ...
Rehinatu Adejumo   +3 more
doaj   +1 more source

Herlyn-Werner-Wunderlich syndrome with pyohematocolpos: a case report and review of literature [PDF]

open access: yes, 2023
Herlyn-Werner-Wunderlich syndrome (HWWS) is a rare malformation syndrome of the women reproductive tract characterized by uterus didelphys with obstructed hemivagina and ipsilateral renal agenesis. We report here a case of a 20 year-old patient presented
Habek, Dubravko   +3 more
core   +2 more sources

Stevens-Johnson syndrome with vulvar involvement: A case report and literature review

open access: yesCase Reports in Women's Health, 2022
Stevens-Johnson syndrome is a rare, life-threatening mucocutaneous condition causing necrosis and detachment of the epidermis. Vulvovaginal involvement, seen in up to 70% of affected women, can lead to painful chronic conditions such as adenosis ...
Jessie Hollingsworth   +4 more
doaj   +1 more source

Long‐term effects of surgically corrected menstrual outflow obstruction: A case–control study

open access: yesInternational Journal of Gynecology &Obstetrics, Volume 165, Issue 1, Page 117-124, April 2024.
Abstract Objective To enhance evidence‐based knowledge on long‐term sequalae in patients with surgically corrected obstructing Müllerian anomalies. Methods This long‐term case–control study included patients with menstrual outflow obstruction due to congenital anomalies of the uterus or vagina, who were at least 18 years old, and for whom 2 years had ...
Lisanne Martens   +4 more
wiley   +1 more source

Vaginoscopic resection of hemivagina, in a 20‐year‐old virgin female with prior misdiagnosis of OHVIRA syndrome as a bicornuate uterus: A case report

open access: yesClinical Case Reports, Volume 12, Issue 3, March 2024.
Key Clinical Message OHVIRA syndrome can be misdiagnosed due to its rarity, resulting in the need for more invasive interventions than vaginoscopy. Also, delayed diagnosis of OHVIRA syndrome can affect patient's quality of life by leading to chronic gynecological diseases such as endometriosis and pelvic inflammatory disease.
Ameneh Haghgoo   +3 more
wiley   +1 more source

Hematocolpos en la infancia. A propósito de un caso

open access: yesCorreo Científico Médico, 2013
El hematocolpos no es común en nuestro medio, sigue a alteraciones en la génesis del aparato genitourinario femenino; entre las cuales, el himen imperforado es la malformación congénita más frecuente. La sintomatología suele ser variable e inespecífica;
Ivonne Espinosa Gómez   +5 more
doaj  

Ascitis fetal aislada idiopática [PDF]

open access: yes, 2015
La ascitis fetal aislada es una entidad comúnmente relacionada a distintas patologías, el diagnóstico final se realiza cuando se han descartado sus múltiples causas. Presentamos el caso de una ascitis fetal de causa idiopática, que no tuvo repercusión en
López Vaca, María Fernanda
core  

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