Results 11 to 20 of about 262,079 (155)
Thyroid carcinoma and primary amenorrhea due to Mayer-Rokitansky-Küster-Hauser syndrome: a case report [PDF]
Journal of Medical Case Reports, 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
Piciu Doina +2 more
doaj +3 more sources
Coffin-Siris syndrome with Mayer-Rokitansky-Küster-Hauser syndrome: a case report [PDF]
Journal of Medical Case Reports, 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 +3 more
doaj +3 more sources
SAGE Open Medical Case Reports, 2019 The Mayer-Rokitansky-Küster-Hauser syndrome is the congenital absence or underdevelopment of the uterus and vagina even though the external genitalia, ovaries and ovarian function are normal. This condition is uncommon in Cameroon. A 23-year-old woman of
Thomas Obinchemti Egbe +4 more
doaj +2 more sources
Doença do nó sinusal em paciente jovem com síndrome de Mayer-Rokitansky-Küster-Hauser [PDF]
Journal of Cardiac Arrhythmias, 2017 Relato do caso de uma paciente de 39 anos de idade com síndrome de Mayer-Rokitansky-Küster-Hauser, apresentando doença do nó sinusal e necessidade de implante de marcapasso bicameral.
Marcel Pereira Moussa +3 more
doaj +5 more sources
SINDROME DE MAYER-ROKITANSKY-KÜSTER-HAUSER: EXPERIENCIA CON VAGINOPLASTIA POR TRACCION LAPAROSCOPICA
Revista Chilena de Obstetricia y Ginecología, 2003 Se presenta un caso clínico de síndrome de Mayer-Rokitansky-Küster-Hauser, tratado con vaginoplastia laparoscópicaA clinical case of Mayer-Rokitansky syndrome is presented, treated by vaginal plastic surgery via laparoscopic with ...
Cristián Pomes C., Nicanor Barrena M.
doaj +2 more sources
Annals of Internal Medicine: Clinical CasesWe 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 ...
Ravi Krishnegowda +4 more
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Island Singapore Flap Vaginoplasty of Two Adult Cases of Mayer– Rokitansky–Küster–Hauser Syndrome Type I [PDF]
The Annals of African Surgery, 2019 Mayer–Rokitansky–Küster–Hauser Syndrome Type I is an emotionally distressful rare condition that limits normal sexual functioning and relationships. First described in 1989 by Wee and Joseph, the neurovascular island pudendal thigh flap (Singapore flap ...
Alex Okello Wamalwa +1 more
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Ileum neovaginoplasty for Mayer–Rokitansky–Küster–Hauser: Review and case series
African Journal of Urology, 2017 Objective: To review treatment modalities of Mayer–Rokitansky–Küster–Hauser syndrome, and to present further evidence on the successful use of ileum segment as an additional procedure for the creation of a neovagina.
L. Al-Mehaisen +4 more
doaj +2 more sources
, 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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KIDNEY ON MAYER-ROKITANSKY-KÜSTER-HAUSER SYNDROME [PDF]
, 2014 The Mayer-Rokitansky-Küster-Hauser syndrome (MRKH) is a rare disorder characterized by congenital absence of upper part of the vagina and the absence or atresia of the uterus. The prevalence has been reported as one in 4000-5000 female births.
Breda, Giovanni Luis +2 more
core +1 more source