Turner Syndrome and Fertility

被引:21
|
作者
Viuff, Mette [1 ,2 ]
Gravholt, Claus H. [1 ,3 ]
机构
[1] Aarhus Univ Hosp, Dept Mol Med, Aarhus N, Denmark
[2] Aarhus Univ Hosp, Dept Gynaecol & Obstet, Aarhus N, Denmark
[3] Aarhus Univ Hosp, Dept Endocrinol, Aarhus, Denmark
关键词
Ovarian dysgenesis; Estradiol; Testosterone; Infertility; Cryo preservation; Anti mullerian hormone; Inhibin B; ANTI-MULLERIAN HORMONE; PRIMARY OVARIAN INSUFFICIENCY; PUBERTAL DEVELOPMENT; AORTIC DISSECTION; OOCYTE DONATION; RISK-FACTORS; WOMEN; PREGNANCY; OUTCOMES; FOLLICLES;
D O I
10.1016/j.ando.2022.06.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Turner syndrome (TS) is tightly associated with hypergonadotropic hypogonadism and ovarian dysgene-sis, typically resulting in infertility in the great majority of patients. Therefore females with TS are usually treated with female sex steroids from 11-12 years of age until the normal age of natural menopause of around 53-54 years of age. Infertility is rated among females with TS as a distressing concern and a detrac-tor from a good quality of life. Options for motherhood for females with TS has expanded during recent years. Originally, only adoption was an option, unless of course for the small minority of TS females that still has ovarian function and are capable of achieving pregnancy through normal means. Oocyte donation has become the mainstream option in many countries and seems to work well, especially if patients have been treated with optimal estrogen and gestagen for a prolonged time before the intervention. It comes with an increased risk of cardiovascular complications and TS oocyte donation pregnancies are viewed as high risk pregnancies necessitating increased vigilance. Oocyte cryopreservation of own oocytes is also becoming an option in a select group of TS and has special challenges. Ovarian tissue cryopreservation is a promising new techniques that has been applied successfully in children with cancer. Currently, several trials are running around the world evaluating this techniques in TS. The genetics and genomics behind the ovarian dysgenesis seen in TS is not understood, but new studies have elucidated global changes in DNA methylation and RNA expression in blood from persons with TS and it is likely that similar changes are present in the ovaries. We still, however, need more thorough research to fully uncover the genetic background of ovarian failure in TS. Gene expression studies and methylation analysis from ovarian TS tissues still needs to be performed. (C) 2022 Les Auteurs. Publie par Elsevier Masson SAS.
引用
收藏
页码:244 / 249
页数:6
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