Mother and child with osteogenesis imperfecta type III. Pregnancy management, delivery, and outcome

IF 0.1 Q4 OBSTETRICS & GYNECOLOGY
B. Hüner, Annette Handke-Vesely, K. Lato, Andrea Korzoum, W. Janni, F. Reister
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Abstract

Abstract Objectives Thanks to the advances of modern medicine it has become possible to reach a fertile age even in the case of serious illnesses, enabling those patients to realize their desire to have children. This is also the case with the extremely heterogeneous, often autosomal dominantly inherited osteogenesis imperfecta. Due to a disruption in collagen synthesis those patients are faced with multiple fractures, spinal deformities and a decrease in pulmonary capacity throughout the course of their lives, depending on the subtype and severity of the disease. Obstetricians as well as anesthetists face major interdisciplinary challenges in the case of a pregnancy in those patients because of pregnancy-associated risks like uterine rupture, preterm birth and postpartum hemorrhage as well as risks associated with the nature of osteogenesis imperfecta itself, like bone fractures, spinal deformities and decreased mobility in the course of the progressing pregnancy. Mode of delivery should be planned individually in order to minimize maternal morbidity and mortality. In cases in which the fetus is as well affected by the disease, this aspect must be taken into consideration when it comes to supervision of pregnancy and planning of the birth mode. Case presentation We report the case of a woman with osteogenesis imperfecta type III who spontaneously conceived a pregnancy with a fetus who was also affected by the genetic disease. This constellation has up to now been reported by only few sources and requires supervision by an experienced perinatal center. Conclusions Osteogenesis imperfecta is not an exclusion diagnosis for family planning and a successful delivery. Nevertheless, depending on the form of the disease, mother and child can be severely affected by the disturbed collagen synthesis. Each patient has to be individually advised and cared for with the specific risks due to the type of Osteogenesis imperfecta. In the case of type III, due to extreme scoliosis, pelvic deformity and small growth, only a primary cesarean section can be performed.
III型成骨不全症母子。妊娠管理、分娩和结局
摘要目的由于现代医学的进步,即使在患有严重疾病的情况下,也可以达到生育年龄,使这些患者能够实现他们想要孩子的愿望。这也适用于极不均匀的,通常是常染色体显性遗传的成骨不全症。由于胶原蛋白合成的破坏,这些患者在其整个生命过程中都面临着多处骨折、脊柱畸形和肺容量下降的问题,这取决于疾病的亚型和严重程度。产科医生和麻醉师在这些患者怀孕的情况下面临着主要的跨学科挑战,因为与怀孕相关的风险,如子宫破裂、早产和产后出血,以及与成骨不全本身的性质相关的风险,如骨折、脊柱畸形和妊娠过程中活动能力下降。应个别规划分娩方式,以尽量减少产妇发病率和死亡率。在胎儿也受到疾病影响的情况下,在监督怀孕和计划生育方式时必须考虑到这方面。病例介绍我们报告的情况下,妇女与成骨不全III型谁自发怀孕与胎儿谁也受到遗传疾病的影响。到目前为止,只有少数来源报道了这种星座,需要由经验丰富的围产期中心进行监督。结论成骨不全不是计划生育和成功分娩的排除性诊断。然而,根据疾病的形式,母亲和孩子可能会受到胶原蛋白合成紊乱的严重影响。由于成骨不全症的类型,每个患者都必须单独接受建议和照顾。在III型的情况下,由于极端的脊柱侧凸,骨盆畸形和小生长,只能进行初级剖宫产。
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来源期刊
Case Reports in Perinatal Medicine
Case Reports in Perinatal Medicine OBSTETRICS & GYNECOLOGY-
自引率
0.00%
发文量
37
期刊介绍: Case Reports in Perinatal Medicine is a double-blind peer-reviewed journal. The objective of the new journal is very similar to that of JPM. In addition to evidence-based studies, practitioners in clinical practice esteem especially exemplary reports of cases that reveal specific manifestations of diseases, its progress or its treatment. We consider case reports and series to be brief reports describing an isolated clinical case or a small number of cases. They may describe new or uncommon diagnoses, unusual outcomes or prognosis, new or infrequently used therapies and side effects of therapy not usually discovered in clinical trials. They represent the basic concept of experiences for studies on representative groups for further evidence-based research. The potential roles of case reports and case series are: Recognition and description of new diseases Detection of drug side effects (adverse or beneficial) Study of mechanisms of disease Medical education and audit Recognition of rare manifestations of disease.
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