首页> 外文期刊>Journal of Neurocytology: A Journal of Cellular Neurobiology >Holoprosencephaly-Topologic variations in a Liveborn series: A general model based upon MRI analysis.
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Holoprosencephaly-Topologic variations in a Liveborn series: A general model based upon MRI analysis.

机译:Liveborn系列中的前脑脑拓扑变化:基于MRI分析的通用模型。

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We present an MRI-based anatomic analysis of a series of 9 human brains, representing lobar, semilobar and alobar forms of holoprosencephaly. The analysis of these variable forms of the malformation is based upon a topologic systematics established in a prior analysis of a homogeneous set of semilobar malformations. This systematics has the dual advantage that it serves both as a uniform reference for qualitative description and as a quantitative descriptive base for mathematical correlations between parameters of topology and of growth and development. Within this systematics, the prosencephalic midline is divided from caudal to rostral into diencephalic (DD-right and left, subthalamus through suprachiasmatic junction with telencephalon), telencephalic (TT-right and left, suprachiasmatic border of telencephalon midline to hippocampal commissure) and diencephalic-telencephalic (DT-right and left-hippocampal commissure through temporal limb of choroid fissure) segments. The topologic abnormality of the initial semilobar series was expressed in an orderly rostral to caudal gradient along the TT segment. In each malformation, normal midline topology began with a small posterior corpus callosum. Although the topologic anomaly in the present series invariably also involved the TT segment, this involvement was not continuous and was variably associated with anomalies of the DD in 6 and unilaterally of the DT in 1 brain. In the present as well as with the earlier series of HPE malformations but not in "normative brains," total telencephalic growth is strongly correlated with the length of the midline telencephalic segment. We propose that this system of analysis will be sensitive to the developmental stage and locus of expression of genetic and non-genetic determinants of the formal origin of HPE. For all of the present series, karyotype anlyses were normal. Mutations in the Shh and Zic2 genes were excluded in 2 cases.
机译:我们介绍了一系列的9个人类大脑的MRI基于解剖学分析,分别代表大前脑的大叶,半大叶和大叶形式。对这些形式不正确的畸形的分析是基于对同形半叶畸形的先验分析中建立的拓扑系统。该系统学具有双重优势,既可作为定性描述的统一参考,又可作为拓扑参数与增长与发展之间的数学相关性的定量描述基础。在该系统中,前脑中线从尾部到延髓分为双脑性(DD-右和左,丘脑下通过与视神经上视交叉连接),脑神经性(TT-右和左,脑中视上视交叉于脑中线至海马结合处)和双脑-端脑段(通过脉络膜裂隙的颞肢出现DT-右海马连合)。最初的半叶系列的拓扑异常以沿TT段的有序的从尾部到尾部的梯度表示。在每种畸形中,正常的中线拓扑结构均始于小的后体。尽管本系列中的拓扑异常也总是涉及TT段,但这种累及不是连续的,并且与6例DD的异常和1例DT的单侧异常相关。在当前以及早期的一系列HPE畸形中,但在“规范性大脑”中却没有,总脑神经的生长与中线脑神经节的长度密切相关。我们建议,这种分析系统将对HPE正式起源的遗传和非遗传决定因素的表达的发育阶段和位点敏感。对于所有当前系列,核型分析均正常。 Shh和Zic2基因的突变被排除在2例中。

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