Results 101 to 110 of about 1,400,939 (196)
Mayer-Rokitansky-Kuster-Hauser syndrome: Surgical management of two cases [PDF]
, 2010 The Mayer-Rokitansky-Kuster-Hauser (MRKH) Syndrome is a rare anomaly characterized by congenital aplasia of the uterus and vagina in women showing normal development of secondary sexual characters and normal 44 XX karyotype.
Mungadi, L.A +4 more
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A rare case of 46,XX gonadal dysgenesis and Mayer-Rokitansky-Kuster-Hauser syndrome
, 2016 46,XX 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 (MRKH)
Sriharibabu Manne +6 more
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Revista Colombiana de Obstetricia y Ginecología, 2010 Objetivo: el síndrome de Mayer-Rokitansky-Küster-Hauser (MRKH) es una malformación congénita del útero y la parte superior de la vagina en las mujeres que muestran características sexuales secundarias normales y cariotipo 46 XX.
Mario Arturo González-Mariño +1 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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Case Report Mayer-Rokitansky-Kuster-Hauser Syndrome Associated with Severe Inferior Vena Cava Stenosis [PDF]
, 2020 Precis. The postoperative course of a neovagina creation procedure in a young woman with Meyer-Rokitansky-Kuster-Hauser syndrome was complicated, despite prophylaxis, by extensive pelvic deep venous thrombosis secondary to unsuspected severe inferior ...
John Wu +4 more
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Coexistence of Mayer-Rokitansky-Kuster-Hauser syndrome and neurofibromatosis type I
, 2008 Neurofibromatosis type 1 (NF-1) is the most frequently seen form of neurofibromatosis. The characteristic features of this disorder are cafe au lait macules, neurofibromas, axillary and inguinal freckling, Lisch nodules, bone lesions such as sphenoid ...
Cimsit, Guelseren +5 more
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Síndrome de Mayer-Rokitansky-Kuster-Hauser: relato de caso e revisão da literatura
, 2011 Os autores descrevem o caso de uma paciente jovem com amenorreia primária e caracteres sexuais secundários normais. A investigação diagnóstica constatou a ocorrência da síndrome de Mayer-Rokitansky-Kuster-Hauser.
Lucia Antunes Chagas +4 more
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A Review of Mayer Rokitansky Kuster Hauser Syndrome
Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a rare congenital disorder characterized by the absence or underdevelopment of the vagina and uterus, affecting approximately 1 in 4,500 to 1 in 5,000 female infants. Management involves a multidisciplinary approach, including medical, surgical, and psychological interventions. Vaginal dilation therapy,
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Rokitansky-Kuster-Hauser syndrome with ectrodactyly
, 1988 This paper describes an 18-year-old patient with Rokitansky-Kuster-Hauser (R-K-H) syndrome. In this case, apart from the usual alterations associated with the R-K-H syndrome, such as aplasia of the Mullerian ducts, renal agenesis, ectopic kidney and ...
BARTOLOZZI, Pietro +3 more
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, 2002 Mayer-Rokitansky-Kuster-Hauser (MRKH) sendromu, vagina ile uterusun beraberce hipoplazisi olarak bilinmektedir ve 4000-5000 dişi doğumda 1 olarak gözlenmektedir.
Murat Ulukuş +4 more
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