Results 61 to 70 of about 61,327,405 (92)

Abstracts from the 53rd European Society of Human Genetics (ESHG) Conference: Interactive e-Posters. [PDF]

Eur J Hum Genet, 2020
europepmc   +1 more source

A Case of Iron Overload–Associated Hypogonadism and Mayer–Rokitansky–Küster–Hauser Syndrome in a Patient With Thalassemia

We report a rare case of a 22-year-old woman with transfusion-dependent beta-thalassemia major who presented with primary amenorrhea. Work-up revealed dual etiologies: hypogonadotropic hypogonadism attributable to pituitary iron overload and müllerian ...
Nagaraja Kamath, Aditya Chandrashekar, Ravi Krishnegowda, Naveen Kumar, Rishika Das   +4 more
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Síndrome de Mayer-Rokitansky: Presentación de seis casos y revisión de la literatura

, 2000
The digenesia Müller ducts or agenesis of the uterus and vagina, known as Mayer-Rokitansky-Kuster-Hauser syndrome is a disorder of the female reproductive characterized by primary amenorrhea and abnormalities associated with urogenital tract.
MEDINA, Ruth, Rechkemmer Prieto, Adolfo
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Probe-based confocal laser endomicroscopy for prediction of uterine rejection in a patient submitted to live-donor uterus transplantation. [PDF]

Arq Bras Cir Dig
Safatle-Ribeiro AV, Ejzenberg D, Franco FC, Soares Junior JM, Baracat EC, Monteleone PA, Andraus W.   +6 more
europepmc   +1 more source

Case Report: From absolute uterine factor infertility (AUI) to motherhood: the crucial role of psychosocial assessment in the first Italian uterus transplantation case. [PDF]

Front Psychol
Pistorio ML, De Pasquale C, Veroux M, Giaquinta A, Giambra MM, Grasso A, Scollo P, Quattropani MCA, Veroux P.   +8 more
europepmc   +1 more source

Síndrome de Mayer-Rokitansky-Kuster-Hauser: Comunicación de dos casos

Mayer-Rokitansky-Küster-Hauser syndrome (SMRKH) is a congenital pathologycharacterized by aplasia or agenesis of structures that develop from the mullerianducts in genotypically and phenotypically normal females.
Ramírez Cabrera, Juan, Cvetkovic Vega, Aleksandar, Ayala Céspedes, Darwin   +2 more
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Sequenciamento de exoma em pacientes com suspeita clínica de Síndrome de Mayer-Rokitansky-Küster-Hauser [PDF]

Tese (doutorado) — Universidade de Brasília, Faculdade de Ciências da Saúde, Programa de Pós-Graduação em Ciências da Saúde, 2024.A Síndrome de Mayer-Rokitansky-Küster-Hauser (MRKH) é caracterizada por agenesia/hipoplasia do útero e do terço superior do
Cunha, Gabriela Corassa Rodrigues da
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