Cleidocranial dysplasia (CCD) (MIM 119600 ... Loss of both alleles (-/-) leads to a complete absence of bone owing to a lack of osteoblast differentiation. These studies show that haploinsufficiency ...

Cleidocranial dysplasia (CCD) is a rare genetic disorder characterized by skeletal abnormalities, particularly affecting the development of bones and teeth. The condition is primarily linked to ...

Marie-Sainton syndrome or cleidocranial dysplasia is an autosomal-dominant skeletal dysplasia affecting intramembranous ossification. The condition can be diagnosed from the clinicoradiological ...

India Cleidocranial dysplasia is an autosomal-dominant condition characterised by widely patent calvarial sutures, clavicular hypoplasia, supernumerary teeth and short stature. Though it is not a very ...