Hovatta Outi
Karolinska Institutet Karolinska University Hospital K57, SE 141 86 Stockholm, Sweden.
Pediatr Endocrinol Rev. 2012 May;9 Suppl 2:713-7.
Normal numbers of oocytes and ovarian follicles develop to the ovaries during the first half of the fetal life. The oocytes then start gradually disappearing. Abnormal meiotic division due to the lack of a paring X-chromosome has been suggested as the causative factor. A large proportion, 40-50% of Turner girls have at least some pubertal development, and about 10% may undergo menarche. Ovarian follicles have been found in some 40% of teenagers with Turner syndrome. Serum concentrations of antimullerian hormone (AMH) and follicle stimulation hormone (FSH), karyotype with mosaicism or structural chromosomal abnormalities, and spontaneous onset of pubertal development are positive prognostic signs for the presence of oocytes and ovarian function. Spontaneous pregnancies occur in some 2-10% of Turner women, a higher number than estimated earlier. This is probably due to failed identification of the syndrome among Turner women with ovarian function. Premature ovarian failure (POF) at some age can be expected in most of Turner women. FSH-stimulated oocyte retrieval and IVF can be carried out before predicted POF. Counseling not to postpone childbearing unnecessarily is advisable. Collected oocytes can be cryopreserved using vitrification, and stored until a pregnancy is desired. Large number of primordial oocytes within ovarian follicles can be stored in within superficial biopsied pieces of ovarian cortical tissue, for transplantation back to the ovary later on. Oocyte donation is an effective infertility treatment for Turner women who have undergone POF. Adequate hormonal replacement therapy (HRT) before IVF is necessary. Only one embryo at a time should be transferred particularly to these women in order to avoid pregnancy complications. Pregnancies in Turner syndrome women have high risks. Comprehensive health control including MRI of the aorta is recommended already before a planned pregnancy, and aorta has to be followed up by echography at least twice during the pregnancy to evaluate the risk of aortic dissection. Some 30% of Turner women develop hypertension during pregnancy, but this is also common among all oocyte donation pregnancies.
在胎儿期的前半段,卵巢中会发育出正常数量的卵母细胞和卵泡。之后,卵母细胞开始逐渐消失。有观点认为,由于缺乏配对的X染色体导致减数分裂异常是其致病因素。很大一部分(40 - 50%)特纳综合征女孩至少有一些青春期发育,约10%可能会经历初潮。在约40%的特纳综合征青少年中发现了卵巢卵泡。抗苗勒管激素(AMH)和促卵泡生成素(FSH)的血清浓度、存在嵌合体或染色体结构异常的核型以及青春期发育的自然 onset是卵母细胞存在和卵巢功能的阳性预后指标。约2 - 10%的特纳综合征女性会自然受孕,这一数字高于早期估计。这可能是由于在有卵巢功能的特纳综合征女性中未识别出该综合征。大多数特纳综合征女性在某个年龄可能会出现卵巢早衰(POF)。在预测的卵巢早衰之前,可以进行促卵泡生成素刺激下的卵母细胞采集和体外受精(IVF)。建议进行咨询,避免不必要地推迟生育。采集到的卵母细胞可以使用玻璃化冷冻保存,直至有怀孕需求时再取出。卵巢卵泡内大量的原始卵母细胞可以储存在卵巢皮质组织的浅表活检碎片中,以便日后移植回卵巢。卵母细胞捐赠是对已发生卵巢早衰的特纳综合征女性有效的不孕治疗方法。在进行体外受精之前,需要进行充分的激素替代疗法(HRT)。对于这些女性,每次应仅移植一个胚胎,以避免妊娠并发症。特纳综合征女性怀孕有很高的风险。建议在计划怀孕前就进行包括主动脉磁共振成像(MRI)在内的全面健康检查,并且在孕期至少通过超声心动图对主动脉进行两次随访,以评估主动脉夹层的风险。约30%的特纳综合征女性在孕期会出现高血压,但这在所有卵母细胞捐赠妊娠中也很常见。