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sj-docx-4-hpq-10.1177_13591053231199253 – Supplemental material for Issues of identity, perceptions and isolation: An interpretative phenomenological analysis of women’s experience of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome

open access: yes, 2023
sj-docx-4-hpq-10.1177_13591053231199253 for Issues of identity, perceptions and isolation: An interpretative phenomenological analysis of women’s experience of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome by Rebecca Gilfillan and Pelham Carter in ...
Rebecca Gilfillan (17070078)   +1 more
core   +1 more source

sj-docx-2-hpq-10.1177_13591053231199253 – Supplemental material for Issues of identity, perceptions and isolation: An interpretative phenomenological analysis of women’s experience of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome

open access: yes, 2023
sj-docx-2-hpq-10.1177_13591053231199253 for Issues of identity, perceptions and isolation: An interpretative phenomenological analysis of women’s experience of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome by Rebecca Gilfillan and Pelham Carter in ...
Rebecca Gilfillan (17070078)   +1 more
core   +1 more source

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

Радиологические характеристики синдрома Mayer-Rokitansky-Küster-Hauser [PDF]

open access: yes, 2016
IMSP Institutul Mamei şi Copilului, Universitatea de Stat de Medicină şi Farmacie ”Nicolae Testemiţanu”The authors present the results of the use of magnetic resonance imaging (MRI) and spiral computed tomography (SCT) to establish variants of the Mayer ...
Mişina, Ana, Rotaru, Natalia
core   +1 more source

Mayer-Rokitansky-Küster-Hauser syndrome

open access: yesJKS (Jurnal Kedokteran Syiah Kuala), 2020
Abstrak. Mayer–Rokitansky–Küster–Hauser syndrome (MRKH) adalah suatu sindrom yang ditandai dengan aplasia uterus, serviks, dan 2/3 vagina bagian atas karena perkembangan yang tidak sempurna dari duktus Mullerian.
Cut Meurah Yeni   +2 more
doaj   +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

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

Mayer-Rokitansky-Küster-Hauser-Syndrom

open access: yes
Das Mayer-Rokitansky-Küster-Hauser-Syndrom (MRKH) ist eine einschneidende Diagnose für Jugendliche mit weitreichenden Konsequenzen. Das MRKH-Syndrom wird meist entdeckt durch das Ausbleiben der Menstruation in der Pubertät und wird in zwei Formen ...
Betschart, Cornelia; https://orcid.org/   +1 more
core   +2 more sources

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 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

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