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单侧闭合性唇裂脑回畸形伴视隔发育不良。

Unilateral closed lip schizencephaly with septo-optic dysplasia.

作者信息

Bhatnagar S, Kuber R, Shah D, Kulkarni Vm

机构信息

Department of Radio-diagnosis, Padmashree Dr. D. Y. Patil Hospital and Research Centre, Pimpri, Pune, Maharashtra, India.

出版信息

Ann Med Health Sci Res. 2014 Mar;4(2):283-5. doi: 10.4103/2141-9248.129065.

Abstract

Schizencephaly is a rare malformation of the central nervous system. Both genetic and non-genetic etiologies like prenatal infections or ischemia have been postulated. Clinical manifestations most often include varying degrees of developmental delay, motor impairment and seizures. It can be associated with septo-optic dysplasia (SOD), optic nerve hypoplasia and absence of septum pellucidum, pachygyria, polymicrogyria, heterotopia and arachnoid cysts. We report a case of unilateral closed lip schizencephaly with SOD.

摘要

脑裂畸形是一种罕见的中枢神经系统畸形。已推测其病因包括遗传和非遗传因素,如产前感染或局部缺血。临床表现通常包括不同程度的发育迟缓、运动障碍和癫痫发作。它可能与视隔发育不良(SOD)、视神经发育不全、透明隔缺如、巨脑回、多小脑回、异位症和蛛网膜囊肿有关。我们报告一例伴有视隔发育不良的单侧闭合性唇脑裂畸形病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c73/3991957/f8f92e4ff6bd/AMHSR-4-283-g001.jpg

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