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

