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脊髓脊膜膨出(存档)

Meningomyelocele(Archived)

作者信息

Sahni Mitali, Alsaleem Mahdi, Ohri Abhinav

机构信息

Drexel University College of Medicine

University of Kansas /Children's Mercy Hospital

Abstract

Meningomyelocele or myelomeningocele, commonly known as open spina bifida is a devastating congenital malformation of the central nervous system and is associated with significant morbidity and mortality. Neural tube defects are of two types: : Open neural tube defect means that the defect is either not covered at all or just covered by a membrane. It comprises about 80% of all neural tube defects. Closed neural tube defect: No apparent defect externally, usually result from a defect either in the fat, bone, or membranes covering the spinal cord. . Myelomeningocele is the most common open neural tube defect. It is characterized by failure of the neural tube to close in the lumbosacral region during embryonic development (fourth-week post-fertilization), leading to the herniation of the meninges and spinal cord through a vertebral defect. The neural tube fusion starts at the level of the hindbrain (medulla and pons) and progresses rostrally and caudally. Incomplete fusion caudally leads to the formation of meningomyelocele around day 26 of gestation.

摘要

脊髓脊膜膨出,通常称为开放性脊柱裂,是一种严重的中枢神经系统先天性畸形,与显著的发病率和死亡率相关。神经管缺陷有两种类型:开放性神经管缺陷是指缺陷根本没有被覆盖或仅被一层膜覆盖。它约占所有神经管缺陷的80%。闭合性神经管缺陷:外部没有明显缺陷,通常是由于覆盖脊髓的脂肪、骨骼或膜存在缺陷所致。脊髓脊膜膨出是最常见的开放性神经管缺陷。其特征是在胚胎发育期间(受精后第四周)神经管在腰骶部未能闭合,导致脑膜和脊髓通过椎体缺陷疝出。神经管融合始于后脑(延髓和脑桥)水平,并向头端和尾端进展。妊娠第26天左右,尾部融合不完全会导致脊髓脊膜膨出的形成。

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