Results 11 to 20 of about 1,400,939 (196)
Mayer–Rokitansky–Kuster–Hauser syndrome: Recent clinical and genetic findings
Gynecological Endocrinology, 2009 Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is characterized by Mullerian duct aplasia in an XX individual with female phenotype presenting primary amenorrhea at adolescence. Multiple abnormalities may be associated with the MRKH syndrome. Genetic investigations focused on the genes of anti-Mullerian hormone and its receptor, as well as on Wt1, Pax2,
Pascal Philibert, Anna Biason-Lauber
exaly +4 more sources
Gonadal Dysgenesis 46, XX Associated with Mayer-Rokitansky-Kuster-Hauser Syndrome: One Case Report [PDF]
Obstetrics and Gynecology International, 2010 Introduction. The association of gonadal dysgenesis and Mayer-Rokitansky-Kuster-Hauser syndrome is very rare and appears to be coincidental, independent of chromosomal anomalies. Case Report.
N. Bousfiha +5 more
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MRI in the diagnosis of Mayer-Rokitansky-Kuster-Hauser syndrome. [PDF]
Diagnostic and interventional radiology (Ankara, Turkey), 2013 The aim of this study was to establish the role of magnetic resonance imaging (MRI) in patients with Mayer-Rokitansky-Kuster-Hauser syndrome (MRKHS).Sixteen female MRKHS patients (mean age, 19.4 years; range, 11-39 years) were studied using MRI. Two experienced radiologists evaluated all the images in consensus to assess the presence or absence of the ...
Beyhan, Murat +3 more
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MAYER-ROKITANSKY-KUSTER-HAUSER (MRKH) SYNDROME TYPE 2: ATYPICAL PRESENTATION OF RARE CASE [PDF]
National Journal of Medical Research, 2013 Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a congenital malformation characterized by an absence of the vagina associated with a variable abnormality of the uterus and the urinary tract but functional ovaries.
Ashok Nakum +3 more
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Mayer-Rokitansky-Kuster-Hauser Syndrome: A Unique Case Presentation. [PDF]
Military Medicine, 2018 Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a congenital condition characterized by aplasia of the vagina with or without concurrent uterine and/or cervical aplasia. Type II (MURCS) is a rare form involving MUllerian agenesis, Renal agenesis, and Cervicothoracic Somite anomalies.A 17-yr-old virginal female presented for evaluation of primary ...
Katherine Dengler
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MURCS Syndrome: Atypical form of Mayer-Rokitansky-Kuster-Hauser Syndrome. [PDF]
J Obstet Gynaecol IndiaMURCS syndrome stands for mullerian duct aplasia, renal anomalies, and cervicothoracic somite anomalies. This is an atypical manifestation of MRKH (Mayer-Rokitansky-Kuster-Hauser) syndrome and is classified as MRKH type 2. Their usual presentation is for the evaluation of primary amenorrhea, and some may present early for the evaluation of short ...
Katam KK, Satapathy D, Arumulla M.
europepmc +3 more sources
A Novel Association of Colonic Duplication with Mayer–Rokitansky–Kuster–Hauser Syndrome in an Adolescent Girl [PDF]
Journal of Indian Association of Pediatric SurgeonsThe association is defined as two or more malformations with unclear relationships, which do not fit the criteria of a syndrome. This case report presents a rare finding of tubular colonic duplication in association with Mayer–Rokitansky–Küster–Hauser ...
Rajib Bora +4 more
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Mayer-Rokitansky-Kuster-Hauser Syndrome Associated with Severe Inferior Vena Cava Stenosis
Case Reports in Obstetrics and Gynecology, 2014 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 ...
Laura Londra +3 more
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Journal of Human Reproductive Sciences, 2015 Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a rare disorder described as aplasia or hypoplasia of uterus and vagina due to an early arrest in development of mullerian ducts.
Maithili Mandar Kulkarni +3 more
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Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome - a review
Indian Journal of Urology, 2002 Purpose: Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a congenital malformation characterized by an absence of the vagina associated with a variable abnormality of the uterus and the urinary tract butfunc-tional ovaries. We review the embryological, endocrino-logical, clinical, diagnostic, psychosocial and therapeutic features of this syndrome ...
N P Gupta, M S Ansari
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