查询词典 corpus callosum

In about 90% of those with apparently isolated agenesis of the corpus callosum deelopment is normal.

预后：取决于病因，90%明显的单纯性胼胝体发育不全是正常的。

Several cases of congenital agenesis of the corpus callosum have been reported in the literature, and it is clear that this deformity need not result in language learning difficulties.

据文献上的报导，有几个先天胼胝体发育不全的案例，而这种缺陷对导致语言学习的困难不是必要的。

Agenesis of the corpus callosum is found in about 5 per 1,000 births.

病因：发育不良或破坏性损伤的继发表现。

ObjectiveTo assess the value of three-dimensional ultrasonography in the prenatal diagnosis of fetal agenesis of the corpus callosum.

目的 探讨三维超声在胎儿胼胝体发育不良(agenesis of the corpus callosum，ACC)产前诊断中的应用价值。

Patients with mech-anical injuries to corpus callosum, e,g., tumor compression, anterior or posterior cerebral artery infarction may have in neurological defects including left apraxia, left alexia or anomia to colors. Nevertheless, these symptoms may not occur in congenital corpus callosum agenesis, complete or incomplete.

胼胝体的后天缺损常造成患者左侧失用症及左侧失读症等右大脑无法取得左大脑资讯的症状；然而先天性胼胝体完全或部分缺损（complete or incomplete congenital corpus callosum agenesis）却不见得会有这些症状，相对的，它伴随其他症候群的机会则很大。

The commissure that is located just inferior to the anterior tip of the corpus callosum; a major route of communication between the left and right temporal lobe.

这个接合处是落在 corpus callosum 下方和前方的顶端，是左右颞叶沟通的主要途径。

The corpus callosum is not isible in the standard transerse iews of the brain but agenesis of the corpus callosum may be suspected by the absence of the caum septum pellucidum and the 'teardrop' configuration of the lateral entricles (enlargement of the posterior horns).

诊断：正常在脑的标准横切面上看不到胼胝体，通常通过透明隔腔小时和侧脑室的泪滴状改变怀疑有胼胝体的发育不良，确诊胼胝体发育不良需要在正中冠状面和正中矢状面上，一般需要做阴道B超显示。

Of the 19 cases,19 fetus were found,MRI confirmed 14 cases considered or suspected as fetal corpus callosum agenesis by US(8 cases are completed agenesis of corpus collosom-CACC,6 cases are partial agenesis of corpus collosom-PACC, and 5 cases had took on autopsy),however 3 cases are mild enlargement of lateral cerebral ventricle and 2 cases are leukodystrophy.In these cases,MRI confirmed a Dandy-Walker syndrome and a lipoma of corpus callosum suspected by US,detect a Dandy-Walker syndrome and a microcephalus made missed diagnoses by US.The fetal corpus callosum and additional cerebral anomalies were shown more clearly on MR T_2-weighted images.

胎儿胼胝体长度与额枕径的比值在24～36孕龄阶段相对较恒定。2、19例孕妇共检出胎儿19个，MRI证实超声疑诊的胎儿胼胝体发育不全14例(完全型胼胝体发育不全8例，部分型胼胝体发育不全6例，有胎儿尸检结果对照者5例)，3例为单纯侧脑室轻度扩张，2例考虑脑白质发育不良，合并Dandy—Walker综合征1例，胼胝体脂肪瘤1例，检出超声漏诊合并Dandy-Walker综合征1例及脑小畸形1例。

To evaluate normal development and anomalies of corpus callosum in childhood, magnetic resonance images of 149 children and 20 adults with normal findings were collected to measure the thickness of genu, body and splenium and the length of corpus callosum on the midsagittal T1-weighted images.

我们选择脑部磁振造影所见正常之149位病童及20位成人，由T1为主的(T1-weighted)正中矢状面影像，测定胼胝体在膝部、体部及压部之厚度，胼胝体长度，以及脑前后径。

Results: ADC in MS group was increased in all regions of NAWM compared to controls(P＜0.05),significantly higher in the body of corpus callosum, internal capsule, periventricular WM, frontal WM, parietal WM and occipital WM(P＜0.01). FA value in MS group was decreased in the body of corpus callosum, internal capsule, periventricular WM, frontal WM, parietal WM and occipital WM(P＜0.05), the genu and splenium of CC,middle cerebellar peduncle showed an insignificant trend of lower FA.

结果：MS组的正常表现脑白质的ADC值均高于对照组(P＜0.05)，以胼胝体体部、内囊、侧脑室旁及额、顶、枕叶脑白质更为显著(P＜0.01)；MS组的FA值与对照组比较，胼胝体体部、顶、额、枕叶白质及内囊、侧脑室旁发现明显降低(P＜0.05)，以后4个部位更为显著(P＜0.01)，而胼胝体膝部、压部和小脑结合臂有降低趋势，但无统计学意义。

They weren't aggressive, but I yelled and threw a rock in their direction to get them off the trail and away from me, just in case.

他们没有侵略性，但我大喊，并在他们的方向扔石头让他们过的线索，远离我，以防万一。

In slot 2 in your bag put wrapping paper, quantity does not matter in this case.

在你的书包里槽2把包装纸、数量无关紧要。