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Rhombencephalosynapsis as a cause of aqueductal stenosis: An under-recognized association in hydrocephalic children

机译:菱形脑突触是水管狭窄的原因:在脑积水儿童中的一种公认的协会。

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Background: Rhombencephalosynapsis is a rare genetic aberration characterized by variable vermian hypoplasia/aplasia in conjunction with united cerebellar hemispheres. Genetic defects in the isthmic organizer at the mesencephalic-metencephalic junction are presumably responsible for the associated aqueductal stenosis. Objective: We performed a retrospective review of 20 children with rhombencephalosynapsis to evaluate for and emphasize the association of aqueductal stenosis and hydrocephalus. Materials and methods: We retrospectively reviewed the MR and CT images of 20 children (0-11 years old) with rhombencephalosynapsis encountered at two academic children's hospitals. Rhombencephalosynapsis spectrum severity was graded based on pre-existing literature. We analyzed examinations for ventriculomegaly and degree of aqueductal stenosis. The collicular distances were measured from the collicular apices. Imaging studies were also analyzed for malformations of cortical and cerebellar development. Results: Thirteen of the 20 children (65%) with rhombencephalosynapsis presented with clinical or imaging evidence of hydrocephalus and aqueductal stenosis, principally involving the caudal cerebral aqueduct. All children with aqueductal stenosis had collicular fusion. All six children with complete rhombencephalosynapsis had aqueductal stenosis. The cerebral aqueduct varied from normal to stenotic in children with incomplete rhombencephalosynapsis. Corpus callosum dysgenesis was present in four children. Conclusion: Aqueductal stenosis in the setting of rhombencephalosynapsis is an under-recognized cause of noncommunicating hydrocephalus. Our findings support the hypothesis that a defect involving the common gene(s) responsible for the differentiation and development of both the roof plate and midline cerebellar primordium at the mesencephalon/first rhombomere junction may be responsible for the association of aqueductal stenosis and rhombencephalosynapsis.
机译:背景:菱形脑突触是一种罕见的遗传畸变,其特征是可变的Vermian发育不全/轻瘫和统一的小脑半球。中脑-中脑交界处的峡部组织器中的遗传缺陷可能与相关的导水管狭窄有关。目的:我们对20例菱形脑突触患儿进行了回顾性评估,以评估并强调水管狭窄与脑积水的关系。材料和方法:我们回顾性研究了两家儿童医院中20例(0-11岁)患有菱脑突触的儿童的MR和CT图像。菱形脑突触频谱严重程度根据现有文献进行分级。我们分析了脑室肥大和导水管狭窄程度的检查。从胶体顶点测量胶体距离。影像学研究还分析了皮层和小脑发育的畸形。结果:20名患菱脑突触的儿童中有13名(65%)表现出脑积水和导水管狭窄的临床或影像学证据,主要累及尾脑导水管。所有患有导水管狭窄的儿童均发生了胶质融合。全部六个患有完全性菱脑突触的儿童均患有导水管狭窄。不完全菱形脑突触患儿的脑导水管从正常到狭窄不等。四名儿童中出现call体发育不全。结论:菱形脑突触背景下的导水管狭窄是人们未认识到的非沟通性脑积水的原因。我们的研究结果支持以下假设:涉及中脑/第一个菱形交界处的顶板和中线小脑原基的分化和发育的共同基因缺陷可能是导致水管狭窄和菱形脑突触的原因。

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