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与大型脊髓脊膜膨出和严重肢体缺陷相关的脐膨出-泄殖腔外翻-肛门闭锁-脊柱裂(OEIS综合征)的围产期特征。

Perinatal features of omphalocele-exstrophy-imperforate anus-spinal defects (OEIS complex) associated with large meningomyeloceles and severe limb defects.

作者信息

Chen C P, Shih S L, Liu F F, Jan S W, Jeng C J, Lan C C

机构信息

Department of Obstetrics and Gynecology, Mackay Memorial Hospital, Taipei, Taiwan, Republic of China.

出版信息

Am J Perinatol. 1997 May;14(5):275-9. doi: 10.1055/s-2007-994143.

Abstract

Omphalocele-Exstrophy-Imperforate anus-Spinal defects (OEIS complex), a combination of omphalocele, exstrophy of the bladder, an imperforate anus and spinal defects, arises from a single localized defect in the early development of the mesoderm that will later contribute to infraumbilical mesenchyme, cloacal septum, and caudal vertebrae. In this report, we document the perinatal features of two cases of OEIS complex associated with meningomyeloceles and severe lower limb defects, and discuss the prenatal diagnosis, inheritance, and differential diagnosis of this association of malformations. Although long-term survival can be achieved by successful corrective surgery, the associated structural defects such as large meningomyelocele and severe limb aplasia or hypoplasia, as seen in our patient, can influence the patient's quality of life. We would like to emphasize that an accurate prenatal diagnosis of OEIS complex and associated malformations is important for the detailed counseling of the family as well as appropriate perinatal management by the obstetricians, pediatric surgeons, urologists, neurosurgeons, and neonatologists.

摘要

脐膨出-膀胱外翻-肛门闭锁-脊柱裂(OEIS综合征),是脐膨出、膀胱外翻、肛门闭锁和脊柱裂的组合,由中胚层早期发育中的单个局部缺陷引起,该中胚层随后将形成脐下间充质、泄殖腔隔膜和尾椎。在本报告中,我们记录了两例与脊髓脊膜膨出和严重下肢缺陷相关的OEIS综合征病例的围产期特征,并讨论了这种畸形关联的产前诊断、遗传方式及鉴别诊断。尽管通过成功的矫正手术可以实现长期存活,但如我们的患者所见,相关的结构缺陷,如巨大的脊髓脊膜膨出和严重的肢体发育不全或发育不良,会影响患者的生活质量。我们想强调的是,对OEIS综合征及相关畸形进行准确的产前诊断,对于为家庭提供详细咨询以及产科医生、小儿外科医生、泌尿科医生、神经外科医生和新生儿科医生进行适当的围产期管理都很重要。

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