Maternal, fetal and neonatal outcomes among pregnant women with arthrogryposis multiplex congenita: a scoping review.

IF 3.5 2区 医学 Q2 GENETICS & HEREDITY Orphanet Journal of Rare Diseases Pub Date : 2025-03-17 DOI:10.1186/s13023-025-03631-5
Arda Arduç, Johanna I P De Vries, Maria B Tan-Sindhunata, Femke Stoelinga, Remco Jansen, Ingeborg H Linskens
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Abstract

Background: The rarity of pregnancies in women with arthrogryposis multiplex congenita (AMC) could lead to healthcare providers having limited exposure to these cases. Consequently, they may be less familiar with the possibilities and challenges associated with pregnancies in women affected by AMC. AMC is an umbrella term for a disorder with multiple contractures at birth, having a broad spectrum of causes, onset and severity of expression. A clinical classification describing the phenotype is Group 1 with primary limb involvement, Group 2 with musculoskeletal involvement plus other system anomalies, and Group 3 with musculoskeletal involvement plus central nervous system dysfunction and/or intellectual disability. A scoping review was conducted to review available literature on documented cases of pregnancies in women with AMC, with the following aims: (1) to outline the maternal, fetal and neonatal outcomes; (2) to describe AMC stability during and after pregnancy (worsening of symptoms due to contractures, increased muscle weakness, pain or lung involvement); and (3) to summarize counselling aspects during pregnancy for expecting mothers who have AMC.

Results: This scoping review included 27 manuscripts reporting on 43 women with 82 pregnancies, of whom 18 in Group 1, 20 in Group 2, 2 in Group 3, and 3 with an unknown type. Details on pregnancy-related outcomes could be depicted from 26 of the 43 women concerning 31 pregnancies. Among these pregnancies, 74% (23/31) had a cesarean section delivery, of which 74% (17/23) were elective. Children were born preterm before week 37 in 7 of 31 pregnancies (22%). A birth weight below the 10th percentile was seen in 6 of the 24 (25%) with a reported birth weight. The course of the pregnancy was uneventful in 16 of the 26 women (62%). Pregnancy had a limited negative influence on AMC stability except for three cases with a transient worsening of lung function.

Conclusions: Gathering the information of the case histories revealed that the majority of the reported women had Distal Arthrogryposis with stable AMC during pregnancy and after delivery. The risk to have a cesarean section, preterm labour or a small for gestational age child is higher in this group than in the general population. Insights obtained by this review emphasized to offer (pre)pregnancy counselling and care by a multidisciplinary team tailored to the women's type of AMC, to ensure optimal preparation for both obstetric, genetic, neurologic, pulmonary and anesthetic care during pregnancy, delivery and postpartum period.

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多重先天性关节挛缩症孕妇的母体、胎儿和新生儿结局:一项范围综述。
背景:患有多重先天性关节挛缩症(AMC)的妇女很少怀孕,这可能导致医疗保健提供者对这些病例的接触有限。因此,他们可能不太熟悉受AMC影响的妇女怀孕的可能性和挑战。AMC是一种先天性多挛缩疾病的总称,具有广泛的病因、发病和表现的严重程度。描述表型的临床分类为1组伴有原发性肢体受累,2组伴有肌肉骨骼受累加上其他系统异常,3组伴有肌肉骨骼受累加上中枢神经系统功能障碍和/或智力残疾。我们进行了一项范围综述,以回顾现有文献中记录的患有AMC的妇女怀孕病例,目的如下:(1)概述母体、胎儿和新生儿的结局;(2)描述妊娠期间和妊娠后AMC的稳定性(因挛缩、肌肉无力加重、疼痛或肺部受累等症状加重);(3)总结患有AMC的准妈妈在怀孕期间的咨询问题。结果:本综述纳入了27篇文献,报告了43例82例妊娠,其中18例为1组,20例为2组,2例为3组,3例为未知类型。43名妇女中有26名涉及31次怀孕,详细描述了与怀孕有关的结果。在这些孕妇中,74%(23/31)采用剖宫产,其中74%(17/23)为选择性分娩。31例妊娠中有7例(22%)在37周前早产。24例报告出生体重的患者中有6例(25%)出生体重低于第10百分位。26名妇女中有16名(62%)的妊娠过程平安无事。除了3例肺功能短暂恶化外,妊娠对AMC稳定性的负面影响有限。结论:收集病例史信息显示,大多数报告的女性在妊娠和分娩期间患有远端关节挛缩并伴有稳定的AMC。在这一群体中,剖腹产、早产或小于胎龄儿童的风险高于一般人群。本综述所获得的见解强调提供(孕前)咨询和护理由一个多学科团队量身定制的女性AMC类型,以确保在怀孕,分娩和产后期间的产科,遗传,神经学,肺和麻醉护理的最佳准备。
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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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