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塞伊-杰拉尔德(VATER)综合征中的神经缺陷。

Neural defects in Say-Gerald (VATER) syndrome.

作者信息

Aleksic S, Budzilovich G, Greco M A, Reuben R, Feigin I, Pearson J

出版信息

Childs Brain. 1984;11(4):255-60. doi: 10.1159/000120185.

Abstract

The Say-Gerald (VATER) syndrome consists of vertebral defects, anal atresia, tracheoesophageal fistula, radial dysplasia and renal defects. 2 children with Say-Gerald (VATER) syndrome were autopsied: the first child was found to have hydrocephalus, aqueductal stenosis and probable craniosynostosis, and the second child had hypoplasia of the nerve roots and anterior and posterior horns of the spinal cord, corresponding to the hypoplastic limb. It is suggested that the Say-Gerald syndrome is a multifocal developmental disorder in which central nervous system anomalies may be found. The children with Say-Gerald syndrome should have a complete neurological examination in order to rule out a potentially treatable central nervous system defect.

摘要

塞-杰拉尔德(VATER)综合征包括脊柱缺损、肛门闭锁、气管食管瘘、桡骨发育不全和肾脏缺损。对2例塞-杰拉尔德(VATER)综合征患儿进行了尸检:首例患儿发现有脑积水、导水管狭窄和可能的颅缝早闭,第二例患儿脊髓神经根及前角和后角发育不全,与发育不全的肢体相对应。提示塞-杰拉尔德综合征是一种多灶性发育障碍,可能存在中枢神经系统异常。患有塞-杰拉尔德综合征的儿童应进行全面的神经系统检查,以排除潜在可治疗的中枢神经系统缺陷。

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