Results 51 to 60 of about 61,328,346 (89)
Síndrome de Mayer-Rokitansky-Küster-Hauser o agenesia de útero y vagina en una paciente joven [PDF]
, 2018 The case report of a patient with syndrome of Mayer-Rokitansky-Küster-Hauser or uterus and vagina agenesis, but with functioning ovaries, assisted by a multidisciplinary team in "Tamara Bunke Bider" Northern Maternal Hospital in Santiago de Cuba, whose ...
Orozco Hechavarría, Nélida +2 more
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Clinical case: Mayer-Rokitansky-Kuster-Hauser syndrome, atypic form [PDF]
, 2011 Secţia Urologie IMSP SCM „Sf. Treime”, Catedra Urologie şi Nefrologie Chirurgicală, USMF „N. Testemiţanu”, Al V-lea Congres de Urologie, Dializă şi Transplant Renal din Republica Moldova cu participare internaţională (1-13 iunie 2011)Summary.
Chiriţa, Lilia +6 more
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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 +2 more
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, 2019 Data for: Detection of De novo Genetic Variants in Mayer-Rokitansky-Küster-Hauser syndrome by Whole Genome ...
hongxin pan (7184819)
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Mayer-Rokitansky-Kuster-Hauser syndrome (a clinical case)
, 2017 Congenital aplasia of the uterus and vagina occurs from 1 in 5000 to 1 in 20000 among newborn girls. Clinical case. A 16-year-old patient A. was admitted to the Regional Children’s Clinical Hospital No.1 of the Department of Obstetrics, Gynecology and ...
Pilipenko, Natalia, Romanova, Natalia
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Creation of a Neovagina by Laparoscopic Modified Vecchietti Technique: Anatomic and Functional Results. [PDF]
Rev Bras Ginecol Obstet, 2016 Baptista E +4 more
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Mayer-Rokitansky-Kuster-Hauser syndrome: a review
, 2015 Laura Londra, Farah S Chuong, Lisa KolpDivision of Reproductive Endocrinology and Infertility, Department of Gynecology and Obstetrics, Johns Hopkins University, Baltimore, MD, USAAbstract: The congenital aplasia or severe hypoplasia of mullerian ...
Chuong FS, Londra L, Kolp L
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, 2012 Introduction: The Mayer-Rokitansky-Küster-Hauser syndrome is characterized by the absence of the vagina and uterus and primary amenorrhea. Objective: The diagnostic evaluation and the therapeutic possibilities of a rare syndrome. Materials and methods:
DEL MAR MUÑOZ, MARÍA +2 more
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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
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Abstracts from the 53rd European Society of Human Genetics (ESHG) Conference: Interactive e-Posters. [PDF]
Eur J Hum Genet, 2020 europepmc +1 more source