Results 31 to 40 of about 61,327,405 (92)

Coffin-Siris syndrome with Mayer-Rokitansky-Küster-Hauser syndrome: a case report [PDF]

open access: yes, 2010
Introduction We report the case of an unusual association of Coffin-Siris syndrome with Mayer-Rokitansky-Küster-Hauser syndrome. This association has never previously been reported in the medical literature.
Shukla Umesh   +7 more
core   +2 more sources

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

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

Thyroid carcinoma and primary amenorrhea due to Mayer-Rokitansky-Küster-Hauser syndrome: a case report [PDF]

open access: yes, 2012
Introduction This case report describes an association between an exceptionally rare congenital anomaly and differentiated thyroid carcinoma. Mayer-Rokitansky-Küster-Hauser syndrome is characterized by vaginal aplasia associated with other Müllerian duct
Alexandru Irimie   +5 more
core   +2 more sources

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

Síndrome de Mayer-von Rokitansky-Küster-Hauser

open access: yesRevista Universitas Medica, 2013
Introducción: el síndrome de Mayer-von Rokitansky-Küster-Hauser (MRKH) ocurre aproximadamente en una de cada cinco mil mujeres nacidas vivas y es la causa más común de ausencia congénita de vagina. Método: se presentan dos casos manejados quirúrgicamente
Gabriel Andrés Barbosa Ramírez   +2 more
doaj  

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

Adolescente con síndrome de Mayer-von Rokitansky-Küster-Hauser: la importancia de un manejo integral multidisciplinario An adolescent suffering from Mayer-von Rokitansky-Küster-Hauser syndrome: the importance of an integral multidisciplinary approach

open access: yesRevista Colombiana de Obstetricia y Ginecología, 2006
Se presenta el caso clásico de una adolescente con diagnóstico incidental y tardío de síndrome de Mayer-von Rokitansky-Küster-Hauser y lo que consideramos aspectos fundamentales a tener en cuenta para favorecer el diagnóstico precoz y manejo de estas ...
Gabriel Barbosa, Mario Varela-Guzmán
doaj  

Descripción de técnica simplificada de neovagina. Reporte de 4 casos: Cali (Colombia) A description of a simplified neovagina technique: A report of 4 cases from Cali, Colombia

open access: yesRevista Colombiana de Obstetricia y Ginecología, 2010
Introducción: la agenesia de vagina representa una malformación infrecuente cuyas principales causas son el síndrome de Rokitansky-Mayer-Kuster-Hauser y la insensibilidad a los andrógenos o síndrome de feminización testicular.
Gustavo Gómez-Tabares   +1 more
doaj  

Perfil clínico e sociodemográfico de um grupo de mulheres brasileiras com a Síndrome de Mayer-Rokitansky-Küster-Hauser

open access: yes
Os dados referem-se a características clínicas e sociodemográficas de um grupo de mulheres brasileiras com diagnóstico de Síndrome de Mayer-Rokitansky-Küster-Hauser assistidas pelo Instituo ...
Lídia Silveira dos Santos
core   +1 more source

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