cleidocranial

cleidocranial的基本解释

-

[医] 锁骨头颅的

与cleidocranial相关的网络例句 [注：此内容来源于网络，仅供参考]

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。

与cleidocranial相关的网络解释 [注：此内容来源于网络，仅供参考]

cleidocranial dysplasia：锁骨颅骨发育不良

cleft palate 颚裂 | cleidocranial dysplasia 锁骨颅骨发育不良 | clinodactyly 小指内弯

cleidocranial dysplasia：锁骨颅骨发育异常

43 Apert syndrome 爱伯特氏症 755.55 | 44 Cleidocranial dysplasia 锁骨颅骨发育异常 755.59 | 45 DiGeorge's syndrome DiGeorge's症候群 279.11

cleidocranial dysplasia：锁骨颅骨发育

cleft palate 颚 | cleidocranial dysplasia 锁骨颅骨发育 | clinodactyly 小指内弯

cleidocranial dysostosis：锁骨颅骨发育不全

锁骨颅骨发育不全(cleidocranial dysostosis)综合征即Marie-Sainton综合征,又名Hulkerantt骨形成不全、Schenthaurer综合征等. 颅锁发育不全的特点是膜内化骨部位的骨化不良,主要发生在锁骨、颅骨和骨盆. 但软骨内化骨也会有些影响,病儿有轻度侏儒表现.