Hellmund Astrid, Berg Christoph, Geipel Annegret, Müller Annette, Gembruch Ulrich
Department of Obstetrics and Prenatal Medicine, University Hospital Bonn, Sigmund Freud-Str. 25, 53105, Bonn, Germany.
Division of Prenatal Medicine, University Hospital Cologne, Cologne, Germany.
Arch Gynecol Obstet. 2016 Oct;294(4):697-707. doi: 10.1007/s00404-016-4017-x. Epub 2016 Jan 29.
Fetal akinesia deformation sequence (FADS) is a clinically and genetically heterogenous disorder. In this study, the different sonographic abnormalities are described in a larger number of affected fetuses.
This retrospective study included 79 cases of suspected FADS observed in our tertiary referral center between January 2001 and February 2015. Electronic stored reports and images of the examination were reviewed as well as autopsy reports and pediatric charts.
In the study population (mean gestational age 23 + 4 weeks) consanguinity, multiple miscarriages or positive family history were present in 31.6 % of cases. Abnormalities of the facial profile (58.3 %) and ankle joint (83.6 %) were detected in the majority of cases. Contractures variably involved knee-, ankle-, wrist- and elbow joint and fingers with no distinct patterns. Additional malformations, most commonly of the brain, were found in 44.3 % of cases. Diagnosis before 20 weeks was associated with nuchal edema in 62.5 and hydrops in 31.3 %. In fetuses evaluated later than 24 weeks, IUGR, increased amniotic fluid or thorax hypoplasia were diagnosed, in 31, 58.8 and 37.9 %, respectively. Termination of pregnancy was requested in 86.1 %, 11 (13.9 %) children were live born. No underlying genetic cause was established, but in one asymptomatic mother myasthenia gravis was revealed.
Fetal akinesia presents with heterogeneous sonographic findings, mostly affecting the profile, elbow-, knee-, ankle joint, wrists and fingers; in most of cases of sporadic nature. Whereas hydrops fetalis and nuchal edema were earlier signs, thorax hypoplasia, polyhydramnios and IUGR were found later in pregnancy.
胎儿运动减少变形序列征(FADS)是一种临床和遗传异质性疾病。在本研究中,对大量受累胎儿的不同超声异常表现进行了描述。
这项回顾性研究纳入了2001年1月至2015年2月在我们的三级转诊中心观察到的79例疑似FADS病例。回顾了电子存储的检查报告和图像以及尸检报告和儿科病历。
在研究人群(平均孕周23 + 4周)中,31.6%的病例存在近亲结婚、多次流产或阳性家族史。大多数病例检测到面部轮廓异常(58.3%)和踝关节异常(83.6%)。挛缩不同程度地累及膝关节、踝关节、腕关节、肘关节和手指,无明显模式。44.3%的病例发现有其他畸形,最常见于脑部。20周前诊断与62.5%的颈部水肿和31.3%的水肿有关。在孕24周后评估的胎儿中,分别有31%、58.8%和37.9%被诊断为宫内生长受限、羊水过多或胸廓发育不全。86.1%的孕妇要求终止妊娠,11名(13.9%)儿童存活出生。未确定潜在的遗传原因,但在一名无症状母亲中发现了重症肌无力。
胎儿运动减少表现为异质性超声表现,主要影响面部轮廓、肘关节、膝关节、踝关节、腕关节和手指;大多数病例为散发性。胎儿水肿和颈部水肿是早期体征,而胸廓发育不全、羊水过多和宫内生长受限在妊娠后期发现。