全前脑畸形——活产系列的拓扑变异:基于MRI分析的一般模型。

T S Takahashi, S Kinsman, N Makris, E Grant, C Haselgrove, S McInerney, D N Kennedy, T A Takahashi, K Fredrickson, S Mori, V S Caviness
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引用次数: 5

摘要

我们提出了一个基于mri的9个人类大脑的解剖分析,代表了前脑全裂症的叶状、半叶状和叶状形式。这些变形的可变形式的分析是基于拓扑系统建立在一组均匀的半叶状畸形的先前分析。这种系统学具有双重优势,既可以作为定性描述的统一参考,又可以作为拓扑参数与生长和发展参数之间的数学相关性的定量描述基础。在这个系统中,前脑中线从尾侧到吻侧分为间脑(dd -左右,丘脑下通过视交叉上与端脑连接)、端脑(tt -左右,端脑中线的视交叉上边界与海马连接)和间脑-端脑(dt -左右海马连接,通过脉络膜裂颞肢)段。最初半叶序列的拓扑异常表现为沿TT节段有序的吻侧到尾侧梯度。在每个畸形中,正常的中线拓扑开始于一个小的后胼胝体。虽然本系列的拓扑异常也无一例外地涉及到TT节段,但这种累及不是连续的,并且与6个脑的DD和1个脑的DT的单侧异常有不同的相关性。在目前以及早期的HPE畸形系列中,但不是在“正常大脑”中,端脑总生长与中线端脑段长度密切相关。我们建议,这一系统的分析将敏感的发育阶段和表达的遗传和非遗传决定因素的HPE正式起源。对于所有本系列,核型分析是正常的。2例排除Shh和Zic2基因突变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Holoprosencephaly--topologic variations in a liveborn series: a general model based upon MRI analysis.

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.

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