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胚胎学、中枢神经系统、畸形

Embryology, Central Nervous System, Malformations

作者信息

Rewane Ayesan, Munakomi Sunil

机构信息

Rush University Medical Center

Kathmandu University

Abstract

The central nervous system (CNS) is composed of the brain and the spinal cord. They both develop from the embryonic ectoderm alongside other structures like the skin. Their development begins as early as the 3rd and 4th weeks of embryonic life, starting with the process of neurulation, which is the development of the neural tube. The neural tube closes spontaneously rostrally and caudally. In the fifth to sixth week, the first appearance of the brain, the prosencephalic development ensues. The primitive brain is comprised of the prosencephalon, mesencephalon, and rhombencephalon. The prosencephalon divides further into telencephalon and diencephalon through a series of developmental stages, namely: formation, cleavage, and development of the midline. Any form of developmental alteration in these leads to the malformation of the developing brain. The article describes the embryology of the central nervous system, the developmental malformation of the cerebral cortex and spinal cord. Developmental malformation of the brain and spinal cord leads to various diseases from microcephaly to spinal bifida. The stages of development of the cerebral cortex encompass three main steps. Defects in one or a combination of these steps form the basis of classification of abnormality of the cortical development as:  an abnormally high proliferation of the neural cells can lead to megalencephaly, and decreased proliferation leads to microcephaly. the outcome of partial neuronal migration is heterotopia and lissencephaly; excessive neuronal migration causes cobblestone malformation. : irregular events in the post-migrational cortical organization causes focal cortical dysplasias and polymicrogyria. The defects of neural tube fusion consist of encephalocele, meningocele, myelomeningocele, and spina bifida occulta. Specifically, alterations in the closure of the rostral neural tube result in conditions like anencephaly or encephalocele. Myelomeningocele occurs from the incomplete causal fusion of the neural tube. Anencephaly typically occurs before the 24th day of life, while encephalocele and myelomeningocele occur about the 26th day of life.

摘要

中枢神经系统(CNS)由脑和脊髓组成。它们与皮肤等其他结构一样,均由胚胎外胚层发育而来。其发育早在胚胎期第3周和第4周就开始了,始于神经胚形成过程,即神经管的发育。神经管会自发地在头端和尾端闭合。在第5至6周,脑首次出现,前脑开始发育。原始脑由前脑、中脑和后脑组成。前脑通过一系列发育阶段进一步分为端脑和间脑,具体包括:中线的形成、分裂和发育。这些过程中任何形式的发育改变都会导致发育中的脑出现畸形。本文描述了中枢神经系统的胚胎学、大脑皮质和脊髓的发育畸形。脑和脊髓的发育畸形会导致从小头畸形到脊柱裂等各种疾病。大脑皮质的发育阶段包括三个主要步骤。这些步骤中一个或多个步骤出现缺陷构成了皮质发育异常分类的基础:神经细胞异常过度增殖会导致巨脑症,而增殖减少会导致小头畸形。部分神经元迁移的结果是异位和无脑回畸形;神经元过度迁移会导致鹅卵石样畸形。迁移后皮质组织中的不规则事件会导致局灶性皮质发育异常和多小脑回畸形。神经管融合缺陷包括脑膨出、脊膜膨出、脊髓脊膜膨出和隐性脊柱裂。具体而言,头端神经管闭合异常会导致无脑畸形或脑膨出等情况。脊髓脊膜膨出是由于神经管的因果融合不完全所致。无脑畸形通常发生在出生后第24天之前,而脑膨出和脊髓脊膜膨出约发生在出生后第26天。

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