Placental insufficiency irrespective of offspring karyotype in maternal Turner syndrome: a case series and literature review.

IF 1.6 4区 医学 Q4 ENDOCRINOLOGY & METABOLISM
Beáta Vida, Gábor Méhes, Olga Török, Mónika Orosz, Zoárd Tibor Krasznai, Attila Jakab, Zsuzsanna Buczkó, Tamás Deli, Péter Juhász
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Abstract

Turner syndrome is one of the most common aneuploidies. In vitro fertilization with oocyte donation is the usual method of assisted conception, but spontaneous pregnancy can also occur. Although pregnancies in Turner syndrome are widely accepted to be associated with small for gestational age foetuses, neither the causal role of placental insufficiency nor the contribution of maternal and foetal factors is well understood. Between 2009 and 2023, we followed 75 patients diagnosed with Turner syndrome at our university clinic, and four Turner syndrome patients became pregnant (4/75; 5.3%): ten pregnancies with seven live births (7/10; 70%) were reported. Conception was spontaneous in 6/7 patients (86%), and one patient had in vitro fertilization with oocyte donation. Two Turner syndrome patients with karyotype 45,X and two Turner syndrome patients with mosaicism (45,X/46,XX) were identified. Prenatal transabdominal amniocentesis revealed aneuploidy (45,X) in two foetuses. The most common obstetric complication was placental insufficiency, which presented as intrauterine growth restriction and foetal distress. Four early-term deliveries, one late-term delivery, one preterm delivery, and one extremely premature delivery occurred, and all pregnancies were terminated by caesarean section. No severe maternal complications during pregnancy were reported. Only newborns with Turner syndrome had long-term health problems. In Turner syndrome patients, even if pregnancy is conceived spontaneously, no maternal complications occur, and the foetus also has a normal karyotype, there is still a high prevalence of placental insufficiency and foetal compromise. The presented cases highlight the possible role of inherent maternal factors in Turner syndrome-associated intrauterine growth restriction and emphasize the importance of enhanced obstetric surveillance even in apparently uncomplicated Turner syndrome pregnancies.

胎盘功能不全与母亲特纳综合征的后代核型无关:一个病例系列和文献综述。
特纳综合征是最常见的非整倍体之一。体外受精与卵母细胞捐赠是辅助受孕的常用方法,但自然妊娠也可能发生。虽然特纳综合征的妊娠被广泛认为与胎龄较小的胎儿有关,但无论是胎盘功能不全的因果作用,还是母体和胎儿因素的贡献,都没有得到很好的理解。2009年至2023年间,我们在我校诊所随访了75名确诊为特纳综合征的患者,其中4名特纳综合征患者怀孕(4/75;5.3%): 10次怀孕,7次活产(7/10;70%)。6/7例患者(86%)自然受孕,1例患者接受卵母细胞捐赠体外受精。发现核型为45、X的特纳综合征患者2例,嵌合型为45、X/46、XX的特纳综合征患者2例。产前经腹羊膜穿刺术显示两个胎儿非整倍体(45,x)。最常见的产科并发症是胎盘功能不全,表现为宫内生长受限和胎儿窘迫。4例早产,1例足月晚期,1例早产,1例极度早产,所有妊娠均通过剖腹产终止。妊娠期未见严重的产妇并发症。只有患有特纳综合症的新生儿才会有长期的健康问题。在Turner综合征患者中,即使自然受孕,未发生母体并发症,胎儿核型也正常,胎盘功能不全和胎儿妥协的发生率仍然很高。提出的病例强调了固有的产妇因素在特纳综合征相关的宫内生长限制中的可能作用,并强调了加强产科监测的重要性,即使在显然不复杂的特纳综合征妊娠中也是如此。
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来源期刊
Archives of Endocrinology Metabolism
Archives of Endocrinology Metabolism Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
2.90
自引率
5.90%
发文量
107
审稿时长
7 weeks
期刊介绍: The Archives of Endocrinology and Metabolism - AE&M – is the official journal of the Brazilian Society of Endocrinology and Metabolism - SBEM, which is affiliated with the Brazilian Medical Association. Edited since 1951, the AE&M aims at publishing articles on scientific themes in the basic translational and clinical area of Endocrinology and Metabolism. The printed version AE&M is published in 6 issues/year. The full electronic issue is open access in the SciELO - Scientific Electronic Library Online e at the AE&M site: www.aem-sbem.com. From volume 59 on, the name was changed to Archives of Endocrinology and Metabolism, and it became mandatory for manuscripts to be submitted in English for the online issue. However, for the printed issue it is still optional for the articles to be sent in English or Portuguese. The journal is published six times a year, with one issue every two months.
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