首页> 外文期刊>American journal of medical genetics, Part A >Malformations of the axial skeleton in Museum Vrolik I: homeotic transformations and numerical anomalies.
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Malformations of the axial skeleton in Museum Vrolik I: homeotic transformations and numerical anomalies.

机译:Vrolik I博物馆中的轴向骨骼畸形:同源变换和数值异常。

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The Museum Vrolik collection of anatomical specimens in Amsterdam, The Netherlands, comprises over 5,000 specimens of human and animal anatomy, embryology, pathology, and congenital anomalies. Recently, we rediagnosed a subset of the collection comprising dried human trunk skeletons and cranial base preparations presenting with homeotic transformations (vertebral phenotypic shifts) and numerical vertebral anomalies. We identified 11 trunk skeletons with either anterior or posterior homeotic transformations (AHT or PHT), 5 trunk skeletons with either less or more than the normal number of vertebrae, and well over a hundred cranial base preparations with either AHT (atlas-assimilation) or PHT (occipital vertebra). We found that, although homeotic transformations and numerical anomalies are distinct conditions, both can be described in terms of mismatch between homeotic patterning and morphological segmentation of the paraxial mesoderm. Therefore these two processes are perhaps not as tightly linked as they may seem on the basis of recent molecular studies. In homeotic transformations there is a constant mismatch between homeotic patterning and morphological segmentation throughout the affected region of the vertebral column. In numerical anomalies there is a variable mismatch between homeotic patterning and morphological segmentation, either because of stretching or squeezing of the homeotic pattern or because of oligo- or polysegmentation of the presomitic mesoderm (PSM). Homeotic transformations of the axial skeleton have an incidence of about 1%-5%, apart from their occurrence in malformation syndromes. Of the various etiological possibilities, explaining their frequent but mostly sporadic occurrence, maternal hyperthermia seems an attractive candidate.
机译:位于荷兰阿姆斯特丹的Vrolik博物馆解剖学标本馆藏包括5,000多种人类和动物解剖学,胚胎学,病理学和先天性异常的标本。最近,我们重新诊断了该集合的一个子集,该子集包括干燥的人躯干骨骼和颅底准备,表现出同种异体转化(椎骨表型转移)和椎体数值异常。我们确定了11个具有前或后顺同性转换(AHT或PHT)的躯干骨架,5个具有少于或大于正常椎骨数量的躯干骨架,以及超过100种具有AHT(图集同化)或PHT(枕椎)。我们发现,尽管同源变换和数值异常是截然不同的条件,但都可以用同源模式和近轴中胚层的形态学分割之间的不匹配来描述。因此,根据最近的分子研究,这两个过程可能并不像看起来那样紧密。在同源转换中,在整个椎柱的受影响区域内,同源图案与形态学分割之间存在恒定的不匹配。在数值异常中,由于顺势图案的拉伸或挤压或者由于早熟中胚层(PSM)的寡节段或多节段,在顺势图案和形态分割之间存在可变的不匹配。除了在畸形综合症中的发生以外,轴向骨骼的同种异体转换的发生率约为1%-5%。在各种病因学可能性中,可以解释其频繁但大多为零星发生的原因,母亲体温过高似乎是一个有吸引力的候选人。

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