Biology of RUNX2 and Cleidocranial Dysplasia

被引:25
作者
Cohen, M. Michael, Jr. [1 ]
机构
[1] Dalhousie Univ, Fac Med, Dept Pediat, Halifax, NS, Canada
关键词
Intramembranous ossification; endochondral ossification; FGF; FGFR; TGF beta; BMP; OSTERIX; TWIST1; Runt domain; haploinsufficiency; MUTATION ANALYSIS; IDENTIFICATION;
D O I
10.1097/SCS.0b013e3182636b7e
中图分类号
R61 [外科手术学];
学科分类号
100210 [外科学];
摘要
Three features of cleidocranial dysplasia that are not always appreciated are hypoplastic iliac wings, short stature, and brachydactyly. Because of the pelvic abnormality, pregnant women may require a cesarean delivery. Short stature and brachydactyly indicate more generalized skeletal abnormalities. These are derived from endochondral and intramembranous ossification, but the distinction between these 2 processes is oversimplified because both processes are involved in long bone and clavicular development. Two sections follow: the biology of RUNX2 and the nature of haploinsufficiency in RUNX2 mutations for cleidocranial dysplasia.
引用
收藏
页码:130 / 133
页数:4
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