- 更多网络例句与无颅畸形相关的网络例句 [注：此内容来源于网络，仅供参考]
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In anencephaly there is absence of the cranial ault with secondary degeneration of the brain.
无脑畸形表现为缺乏颅顶和脑的继发性变性。
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Anencephaly, the single most common open neural tube defect, is characterized by the absence of the cerebral hemispheres and the lack of bony calarium aboe the orbits Fig.
无脑畸形，最常见的单一的开放性神经管缺损，其特点是无大脑半球且没有眼眶以上的骨性颅盖（图10-37A-B和图10-37C）。胎儿有正常的中脑和后颅窝，但大脑半球未正常发育。
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Angiographies were performed in theCEMPs and their angiograms were evaluated in comparison with those of human beings.
结果猪无颈内动脉颅外段，代之以咽升动脉，后者在海绵窦先形成酷似人脑动静脉畸形团的、且两侧网状吻合的微血管网，再汇聚成主要向颅内供血的颈内动脉。
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Chromosomal abnormalities, single mutant genes, and maternal diabetes mellitus or ingestion of teratogens, such as antiepileptic drugs, are implicated in about 10% of the cases.
孕中期诊断无脑畸形基于颅顶和大脑半球缺乏，然而面骨、脑干和部分枕骨、中脑通常存在。大约50%的病例合并脊柱异常，早孕期，可在11周后做出诊断，因为此时，颅骨开始骨化。
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Methods:The depth of the anterior and posterior rims of foramen magnum and the angle between medulla oblongata and upper spinal cord on midsagittal SE or FSE T1WI were measured in 320normal Chinese individuals and in 36patients with basilar impression.
随机选取320例没有颅颈交界区相关的临床症状及体症，MRI扫描无明显颅骨破坏性病变和颅颈交界区畸形的正常国人和36例颅底凹陷症患者的颅脑MRI图像，于正中矢状面SE或FSE T_1WI图像上测量枕大孔前、后缘中点深度和延髓-上颈髓轴线夹角数值。正常人按性别、年龄分16组，每组20例。
- 更多网络解释与无颅畸形相关的网络解释 [注：此内容来源于网络，仅供参考]
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anencephalia：无脑畸形
1.无脑畸形 无脑畸形(anencephalia)是一种严重的DNT,为脑的全部或大部缺如,头颅的缺损从顶部开始,可延伸到其与枕骨大孔的任何部位,患儿因颅骨穹隆缺如造成面部特殊外貌,其前颅窝缩短和眼眶变浅,使眼球向前突出,下颌紧贴胸骨,口半张开,
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anencephaly：无脑畸形
※头颅之畸形的变异甚大,大至裂颅畸形(cranioschisis)与无...脑畸形(anencephaly);而小至需放射线检验方能测得.
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mercury rash：汞疹
Mercurial poisoning; Mercurial rash; Mercurialism; Hydrargyrism 汞中毒; 水银中毒 | Mercury rash 汞疹 | Meroacranial monstrosity; Meroacrany 部份无颅(畸形)
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Acranial monster：无颅畸胎
Acral thickening; Acropachy; Pachyacry 肢端肥厚 | Acranial monster 无颅畸胎 | Acranial monstrosity; Acrany 无颅(畸形)
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Acranial monstrosity; Acrany：无颅(畸形)
Acranial monster 无颅畸胎 | Acranial monstrosity; Acrany 无颅(畸形) | Acrocephalosyndactyly; Apert's syndrom 尖长头并指(趾)(畸形); Apert氏合并症状
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Acrocephalosyndactyly; Apert's syndrom：尖长头并指(趾)(畸形); Apert氏合并症状
Acranial monstrosity; Acrany 无颅(畸形) | Acrocephalosyndactyly; Apert's syndrom 尖长头并指(趾)(畸形); Apert氏合并症状 | Acromegalic giantism 指端肥大症巨大发育
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尖长头并指(趾)(畸形); Apert氏合并症状：Acrocephalosyndactyly; Apert's syndrom
Acranial monstrosity; Acrany 无颅(畸形) | Acrocephalosyndactyly; Apert's syndrom 尖长头并指(趾)(畸形); Apert氏合并症状 | Acromegalic giantism 指端肥大症巨大发育
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cranioschisis：裂颅畸形
※头颅之畸形的变异甚大,大至裂颅畸形(cranioschisis)与无...脑畸形(anencephaly);而小至需放射线检验方能测得.