Literature DB >> 4020785

Müllerian dysgenesis.

R E Varner, J B Younger, R E Blackwell.   

Abstract

The multifaceted syndrome of müllerian dysgenesis appears to represent a defect in mesodermal organization and is often associated with renal and skeletal anomalies. This report discusses the embryology, multifactorial etiology, clinical presentation and management of the syndrome from a historical standpoint and details our experience with 35 affected patients. Both Frank dilatation and McIndoe vaginoplasty appear to be acceptable means of therapy. The therapeutic success depends to a large extent on the psychosocial adaptation of the patient.

Entities:  

Mesh:

Year:  1985        PMID: 4020785

Source DB:  PubMed          Journal:  J Reprod Med        ISSN: 0024-7758            Impact factor:   0.142


  7 in total

1.  The Methods and Mechanisms to Differentiate Endothelial-Like Cells and Smooth Muscle Cells from Mesenchymal Stem Cells for Vascularization in Vaginal Reconstruction.

Authors:  Hua Zhang; Jingkun Zhang; Xianghua Huang; Yanan Li
Journal:  Mol Biotechnol       Date:  2018-06       Impact factor: 2.695

2.  Vaginal reconstruction with sigmoid colon in patients with congenital absence of vagina and menses retention: a report of treatment experience in 22 young women.

Authors:  Bin Yang; Ning Wang; Shulan Zhang; Mingqian Wang
Journal:  Int Urogynecol J       Date:  2012-05-12       Impact factor: 2.894

3.  Utero-vaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome) associated with deletions in known DiGeorge or DiGeorge-like loci.

Authors:  Karine Morcel; Tanguy Watrin; Laurent Pasquier; Lucie Rochard; Cédric Le Caignec; Christèle Dubourg; Philippe Loget; Bernard-Jean Paniel; Sylvie Odent; Véronique David; Isabelle Pellerin; Claude Bendavid; Daniel Guerrier
Journal:  Orphanet J Rare Dis       Date:  2011-03-15       Impact factor: 4.123

Review 4.  The Mayer-Rokitansky-Küster-Hauser syndrome (congenital absence of uterus and vagina)--phenotypic manifestations and genetic approaches.

Authors:  Daniel Guerrier; Thomas Mouchel; Laurent Pasquier; Isabelle Pellerin
Journal:  J Negat Results Biomed       Date:  2006-01-27

Review 5.  Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome.

Authors:  Karine Morcel; Laure Camborieux; Daniel Guerrier
Journal:  Orphanet J Rare Dis       Date:  2007-03-14       Impact factor: 4.123

6.  Rare Case of Leiomyoma and Adenomyosis in Mayer-Rokitansky-Kuster-Hauser Syndrome.

Authors:  P S Hoo; A R Norhaslinda; J N Shah Reza
Journal:  Case Rep Obstet Gynecol       Date:  2016-10-23

7.  Role of HOXA7 to HOXA13 and PBX1 genes in various forms of MRKH syndrome (congenital absence of uterus and vagina).

Authors:  Agnès Burel; Thomas Mouchel; Sylvie Odent; Filiz Tiker; Bertrand Knebelmann; Isabelle Pellerin; Daniel Guerrier
Journal:  J Negat Results Biomed       Date:  2006-03-23
  7 in total

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