查询词典 cleidocranial

This report was to study the morphologic characteristics of dental and face in cleidocranial dysplasia.

锁骨颅骨发育不全综合征(C leidocranial dys-plia，CCD)是一种少见的常染色体显形遗传性疾病。

Objective To investigate the structure and elements of deciduous teeth in a patient with cleidocranial dysplasia.

目的研究颅骨锁骨发育不良(cleidocranial dysplasia，CCD)患者乳牙牙齿结构及组分。

Cleidocranial dysplasia is a rare syndrome usually caused by an autosomal dominant gene without gender predilection.

颅锁骨发育不全是一种罕见体染色体显性遗传的疾病，男女发生的比率相当。

Aberrant function of Runx and CBFβhas been causally related to the development of various diseases,including acute myeloid leukemia,gastric cancer and cleidocranial dysplasia.

RUNX/CBFβ功能的异常已经被发现与许多疾病的发生相关，例如急性髓系白血病、胃癌和颅锁骨发育不全。

Miyamoto A, Shigematsu T, Fukunaga T, et al. Medical baseline data collection on bone and muscle change with space flight［J］. Bone, 1998, 22(5):7982.［2］ Otto F, Thoenell AP, Crompton T, et al. Cbfα1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblasts differentiation and bone development ［J］.

讨论 FSS对成骨细胞功能的影响骨骼按遗传基因的调控建设骨骼的雏形，并在骨的生长发育中根据所承受载荷的需要对自身不断地进行改建与重塑，以试图实现用最小的骨量达到最大的骨强度，这就是骨的功能适应性。

In this article, a case of cleidocranial dysplasia of a 25-year-old Taiwanese female is reported. She visited Taichung Veterans General Hospital Department of Dentistry for the treatment of dental caries in March, 2005. Her abnormalities were diagnosed by Oral and Maxillofacial Surgeon, and was later certified by physician of Genetic Consultation and radiologist.

本文报告一位25岁台湾女性颅锁骨发育不全病例於民国94年三月至台中荣总牙科部寻求龋齿诊治，经口腔颚面外科医师临床及影像检查后，初步臆断为颅锁骨发育不全症候群，后经遗传谘询及放射线部医师确定诊断为颅锁骨发育不良。

Cleidocranial sysplasia ; Dexiduous toogh ; Structure ; Elemaent analysis

颅骨锁骨发育不良综合征；乳牙；结构；能谱分析

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。