Results 31 to 40 of about 1,398,641 (158)

Ovarian dysgerminoma at adolescent with Mayer-Rokitansky-Küster-Hauser syndrome [PDF]

open access: yes, 2018
Introducere. Sindromul Mayer-Rokitansky-Küster-Hauser (MRKH) prezintă o anomalie congenitală multifactorială a ducturilor Mülleriene care se caracterizează prin: (a) agenezia a 2/3 superioare a vaginului, în combinaţie cu anomalia uterului (de la ...
Mişina, Ana   +4 more
core   +1 more source

Coexistence of Gonadal Dysgenesis and Mullerian Agenesis in a Female with 46 XX Karyotype: A Case Report

open access: yesJournal of Nepal Medical Association, 2019
Gonadal dysgenesis is a rare genetically heterogeneous disorder characterized by underdeveloped ovaries with consequent, impuberism, primary amenorrhea, and hypergonadotropic hypogonadism .Mullerian agenesis or Mayer‑Rokitansky‑Kuster‑Hauser syndrome is ...
Santosh Kumar Jha   +2 more
doaj   +1 more source

A rare form of Mayer-Rokitansky-Küster-Hauser syndrome: Case report and review of literature

open access: yesCase Reports in Women's Health, 2019
Introduction: Primary amenorrhea is failure to reach menarche. Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is the second most common cause of primary amenorrhea, after gonadal dysgenesis.
Omran Al Dandan   +4 more
doaj   +1 more source

Hallazgos radiológicos en la agenesia útero ovárica con probable relación a Síndrome Mayer-Rokitansky- Küster- Hauser

open access: yes, 2021
Introducción: La amenorrea es uno de los motivos más comunes en la atención primaria, donde el síndrome de Mayer-Rokitansky-Küster-Hauser se presenta como una anomalía congénita inusual del tracto genital.
Alvarez Mena, Cristian Enrique
core   +1 more source

Manejo laparoscópico de miomatosis uterina en pacientes con Síndrome de Rokitansky: Reporte de un caso y revisión de la literatura

open access: yesRevista Colombiana de Obstetricia y Ginecología, 2013
Introducción: el síndrome de Mayer-Rokitansky-Küster-Hauser (SMRKH) es un espectro de anomalías de los conductos müllerianos caracterizado por la la ausencia congénita de útero y vagina en mujeres fenotípicamente normales, con cariotipo 46 XX, con un ...
Guillermo Páez-López   +7 more
doaj   +3 more sources

Lactation, Childrearing, and Gender Justice

open access: yesJournal of Applied Philosophy, EarlyView.
ABSTRACT In this article, I discuss the significance of early infant feeding choices for the goal of gender justice. Focusing on human lactation practices, I identify Exclusive Gestational Nursing (EGN) as the norm in advanced industrial societies, which creates the expectation and permission for gestators, and only gestators, to nurse children, and ...
Jenny Brown
wiley   +1 more source

Differences in sex development among individuals with a female phenotype and an absent uterus: Diagnostic approach

open access: yesJournal of International Medical Research
Objective To describe individuals with differences in sex development presenting with a female phenotype and an absent uterus and identify specific diagnostic characteristics that improve diagnostic accuracy and optimize patient care.
Ana Jibladze   +3 more
doaj   +1 more source

A Uterus‐Preserving Laparoscopic Technique for Cervicovaginal Agenesis With Functional Uterine Remnants

open access: yesBJOG: An International Journal of Obstetrics &Gynaecology, EarlyView.
ABSTRACT Background Cervicovaginal agenesis with functional uterine remnants is a rare Müllerian anomaly that may cause obstructed menstrual flow, pelvic pain, haematometra, haematosalpinx and endometriosis. Uterus‐preserving reconstruction is challenging because it requires both neovaginal creation and durable uterine drainage.
Kiper Aslan   +3 more
wiley   +1 more source

Dual acellular subnormothermic machine perfusion for enhanced uterus preservation in a swine model

open access: yesActa Obstetricia et Gynecologica Scandinavica, EarlyView.
In a porcine uterus transplantation model, subnormothermic machine perfusion reduced graft edema and better‐preserved post‐reperfusion contractility than static cold storage, highlighting its potential for uterus preservation, assessment, and future graft‐conditioning applications.
Lucile Cabanel   +13 more
wiley   +1 more source

Report and review of described associations of Mayer-Rokitansky-Küster-Hauser syndrome and Silver-Russell syndrome

open access: yes, 2015
Silver–Russell syndrome (SRS) and Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome are described in isolation. However, their co-occurrence has only been rarely reported.
Baynam, Gareth S.   +11 more
core   +2 more sources

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