Sergi C, Hentze S, Sohn C, Voigtländer T, Jung C, Schmitt H P
Institute of Pathology, University of Heidelberg, Germany.
Brain Dev. 1997 Sep;19(6):426-32. doi: 10.1016/s0387-7604(97)00050-8.
Agenesis of the cerebellar vermis (paleocerebellar agenesis) with fusion of the cerebellar hemispheres (rhombencephalosynapsis) is a rare malformation of the central nervous system (CNS). Its combination with synencephaly (telencephalosynapsis), telencephalic ventricular aplasia, aqueductal atresia and cystic fourth ventricle has not yet been described, as far as we know. Here, we report this combination in a 23-weeks' gestation male fetus who was aborted to a 24-year-old diabetic mother. In this fetus with cerebral and cerebellar hemispheric fusion, vermian agenesis was associated with a Dandy-Walker-like posterior fossa cyst, in spite of the fusion of the hypoplastic cerebellar hemispheres. The CNS malformations were further accompanied by dysmorphic facial stigmata such as unilateral atresia of the external ear, ocular hypertelorism and a broad nasal bridge. Preaxial polydactyly and contractures of the upper limbs were the only associated non-cranial abnormalities. Cytogenetic studies revealed a numerically and structurally normal male (46, XY). The malformation complex described in this fetus of a mother with antedating pregnancy diabetes appears to represent a previously undescribed aberrant syngenetic CNS phenotype, some basic teratogenetic aspects of which will be discussed in this paper.
小脑蚓部发育不全(旧小脑发育不全)合并小脑半球融合(菱形脑联合)是一种罕见的中枢神经系统(CNS)畸形。据我们所知,其与无脑回畸形(端脑联合)、端脑室发育不全、导水管闭锁及第四脑室囊肿的合并情况尚未见报道。在此,我们报告一名孕23周的男性胎儿出现了这种合并情况,该胎儿因母亲为一名24岁的糖尿病患者而被引产。在这个脑和小脑半球融合的胎儿中,尽管小脑半球发育不全且融合,但蚓部发育不全与类似丹迪-沃克畸形的后颅窝囊肿相关。中枢神经系统畸形还伴有面部畸形特征,如单侧外耳道闭锁、眼距过宽和鼻梁宽阔。轴前多指畸形和上肢挛缩是仅有的相关非颅脑异常。细胞遗传学研究显示为一名男性,染色体数目和结构正常(46, XY)。本文中描述的这位患有妊娠前糖尿病母亲所产胎儿的畸形复合体似乎代表了一种此前未描述过的异常同基因中枢神经系统表型,本文将讨论其中一些基本的致畸因素。