Add to ORKGCleidocranial dysplasia is a skeletal dysplasia characterized by autosomal dominantinheritance, cranial abnormalities, clavicular, and dental, caused by mutations ordeletions in RUNX2 gene. We report the case of a girl of 6.5 years attended oursubmitted by delayed closure of the anterior fontanelle and ossification of the pelvis, in whom diagnosis is done by clinical and radiological findings.La displasia cleidocraneal es una displasia esquelética de herencia autosómicadominante caracterizada por anomalías craneales, claviculares y dentales, causada por mutaciones o deleciones en el gen RUNX2. Se presenta el caso de una niña de 6,5 años que acude remitida por un retraso en el cierre de la fontanela anterior y en la osificación de la pelvis,...
Background: Cleidocranial dysplasia (CCD) is a rare inherited skeletal dysplasia, with an incidence ...
Copyright © 2012 Radhika Chopra et al. This is an open access article distributed under the Creative...
Cleidocranial dysplasia (CCD) is a rare autosomal dominant skeletal disorder, characterized by delay...
La displasia cleidocraneal es una displasia esquelética de herencia autosómicadominante caracterizad...
Cleidocranial dysostosis (CCD) is a rare congenital bone disorder with an autosomal dominant genetic...
Cleidocranial dysostosis (CCD) is a rare congenital skeletal disorder associated to clavicular hypop...
Cleidocranial dysostosis (CCD) is a rare congenital skeletal disorder associated to clavicular hypop...
Cleidocranial dysplasia (CCD) is a rare syndrome, occurring at a rate of 1:10,000,000 in the form pr...
Abstract Background Cleidocranial dysplasia (CCD) is a rare congenital autosomal dominant skeletal d...
Cleidocranial dysplasia (CCD) is an autosomal dominant skeletal dysplasia associated with cranial, c...
Cleidocranial dysplasia (CCD) is a genetic condition that affects the bones characterized by a tripl...
Cleidocranial dysplasia (Dysostosis) is an autosomal dominant disease with a wide range of expressio...
Background Cleidocranial dysplasia (CCD, #MIM119600) is an autosomal-dominant skeletal dysplasia cha...
Introduction: Cleido-cranial dysplasia (CCD) is a rare congenital disorder with an autosomal dominan...
Cleidocranial dysplasia (CCD) is a rare autosomal dominant skeletal disease, which is caused by muta...
Background: Cleidocranial dysplasia (CCD) is a rare inherited skeletal dysplasia, with an incidence ...
Copyright © 2012 Radhika Chopra et al. This is an open access article distributed under the Creative...
Cleidocranial dysplasia (CCD) is a rare autosomal dominant skeletal disorder, characterized by delay...
La displasia cleidocraneal es una displasia esquelética de herencia autosómicadominante caracterizad...
Cleidocranial dysostosis (CCD) is a rare congenital bone disorder with an autosomal dominant genetic...
Cleidocranial dysostosis (CCD) is a rare congenital skeletal disorder associated to clavicular hypop...
Cleidocranial dysostosis (CCD) is a rare congenital skeletal disorder associated to clavicular hypop...
Cleidocranial dysplasia (CCD) is a rare syndrome, occurring at a rate of 1:10,000,000 in the form pr...
Abstract Background Cleidocranial dysplasia (CCD) is a rare congenital autosomal dominant skeletal d...
Cleidocranial dysplasia (CCD) is an autosomal dominant skeletal dysplasia associated with cranial, c...
Cleidocranial dysplasia (CCD) is a genetic condition that affects the bones characterized by a tripl...
Cleidocranial dysplasia (Dysostosis) is an autosomal dominant disease with a wide range of expressio...
Background Cleidocranial dysplasia (CCD, #MIM119600) is an autosomal-dominant skeletal dysplasia cha...
Introduction: Cleido-cranial dysplasia (CCD) is a rare congenital disorder with an autosomal dominan...
Cleidocranial dysplasia (CCD) is a rare autosomal dominant skeletal disease, which is caused by muta...
Background: Cleidocranial dysplasia (CCD) is a rare inherited skeletal dysplasia, with an incidence ...
Copyright © 2012 Radhika Chopra et al. This is an open access article distributed under the Creative...
Cleidocranial dysplasia (CCD) is a rare autosomal dominant skeletal disorder, characterized by delay...