Literature DB >> 12606594

The N314D polymorphism of the GALT gene is not associated with congenital absence of the uterus and vagina.

S Klipstein1, B Bhagavath, C Topipat, L Sasur, R H Reindollar, M R Gray.   

Abstract

The aetiology of anomalous embryonic and fetal development of the female reproductive tract, ranging from common uterine abnormalities to the somewhat rare congenital absence of the uterus and vagina (CAUV), is unknown. Some have proposed that abnormal galactose metabolism might cause CAUV. An association between CAUV and the N314D allele of the galactose-1-phosphate uridyl transferase (GALT) gene has been proposed as aetiological. We tested this hypothesis further by performing a case-control molecular study analysing 32 patients with CAUV for the presence of the N314D allele. These patients were compared with 138 normal controls. No association between CAUV and the N314D polymorphism was found (P = 0.32). It is unlikely that either maternal or fetal GALT enzyme activity could affect paramesonephric duct development, because neither galactosaemic subjects nor their children have an increased incidence of uterine anomalies.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12606594     DOI: 10.1093/molehr/gag018

Source DB:  PubMed          Journal:  Mol Hum Reprod        ISSN: 1360-9947            Impact factor:   4.025


  11 in total

1.  Identification and functional analysis of a novel LHX1 mutation associated with congenital absence of the uterus and vagina.

Authors:  Wei Zhang; Xueya Zhou; Liyang Liu; Ying Zhu; Chunmei Liu; Hong Pan; Qiong Xing; Jing Wang; Xi Wang; Xuegong Zhang; Yunxia Cao; Binbin Wang
Journal:  Oncotarget       Date:  2017-01-31

2.  Genetic analyses in a variant of Mayer-Rokitansky-Kuster-Hauser syndrome (MURCS association).

Authors:  Gerda Hofstetter; Nicole Concin; Christian Marth; Tuula Rinne; Martin Erdel; Andreas Janecke
Journal:  Wien Klin Wochenschr       Date:  2008       Impact factor: 1.704

3.  Congenital Malformations of the Reproductive Tract in a Patient with Poland Syndrome: Is There a Connection?

Authors:  Tian Meng; Ming Bai; Ru Zhao
Journal:  Breast Care (Basel)       Date:  2017-10-27       Impact factor: 2.860

4.  Genetics of agenesis/hypoplasia of the uterus and vagina: narrowing down the number of candidate genes for Mayer-Rokitansky-Küster-Hauser Syndrome.

Authors:  Sasha Mikhael; Sonal Dugar; Madison Morton; Lynn P Chorich; Kerlene Berwick Tam; Amy C Lossie; Hyung-Goo Kim; James Knight; Hugh S Taylor; Souhrid Mukherjee; John A Capra; John A Phillips; Michael Friez; Lawrence C Layman
Journal:  Hum Genet       Date:  2021-01-19       Impact factor: 5.881

Review 5.  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 6.  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

7.  Genetic Syndromes and Genes Involved in the Development of the Female Reproductive Tract: A Possible Role for Gene Therapy.

Authors:  Mt Connell; Cm Owen; Jh Segars
Journal:  J Genet Syndr Gene Ther       Date:  2013

8.  MURCS Association with Partial Duplication of the Distal Long Chromosome 5 and Unilateral Ovarian Agenesis.

Authors:  Anna Dabkowska-Huc; Piotr Skalba; Antoni Pyrkosz
Journal:  Case Rep Genet       Date:  2013-02-17

Review 9.  Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: a comprehensive update.

Authors:  Morten Krogh Herlin; Michael Bjørn Petersen; Mats Brännström
Journal:  Orphanet J Rare Dis       Date:  2020-08-20       Impact factor: 4.123

10.  Novel Technique of Vaginoplasty Developing Normal Vagina, Role of Stemness Markers and Translational Genes.

Authors:  Pravin Mhatre; Vikas Dighe; Dhanjit Kumar Das; Amol Pawar
Journal:  J Hum Reprod Sci       Date:  2020-12-28
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.