CCD (cleidocranial dysostosis): A genetic (inherited) disorder of bone development characterized by:
The disorder is transmitted in an autosomal dominant manner. A parent with the condition has a 50:50 chance that each of their children will have the condition. Boys and girls stand an equal chance of being affected. The gene for the condition has been found on chromosome 6 (specifically, in band p21). The gene is for the transcription factor CBFA1 (core-binding factor alpha subunit 1). Mutations of CBFA1 cause this disorder.
A possible example of this disorder has been found in the skull of a Neanderthal man.
What is Cleidocranial Dysplasia? Cleidocranial Dysplasia (cleido = collar bone, + cranial = head, + dysplasia = abnormal forming) , also known as Cleidocranial Dysostosis ...
CCD (cleidocranial dysostosis): A genetic (inherited) disorder of bone development characterized by: Absent or incompletely formed collar bones (the "cleido-" part refers ...
CCD (Cleidocranial digital dysostosis) information including symptoms, causes, diseases, symptoms, treatments, and other medical and health issues.
Cleidocranial dysplasia (referred to as CCD in this review) is a skeletal dysplasia ... The term cleidocranial dysostosis has been used; however, given that RUNX2 ...
Cleidocranial Dysplasia (CCD) is also referred to as Marie-Sainton disease or Mutational Dysostosis. This complicated sounding condition medically has the following ...