Add to ORKGBackground: A family case report of cleidocranial dysplasia (CCD) with varied manifestations from father to three siblings is presented. CCD ( MIM # 119600) is a rare autosomal dominant skeletal dysplasia caused by CBAF1 gene ( OMIM 600211) with a wide range of variability. In all the cases generalized dysplasia in bone, prolonged retention of primary teeth and delayed eruption of permanent teeth were evident. Interestingly, there were no supernumerary teeth present. There was mandibular prognathism which was intercepted by occipital chin cup therapy. Aims and objective: To present the clinical manifestations, diagnostic imaging and treatment modalities along with dermatoglyphics in CCD patients. Conclusion: Cleidocranial dysplasia is an un...
Cleidocranial dysplasia (CCD) is a congenital autosomal dominant syndrome characterised by dental an...
Cleidocranial dysplasia (CCD) is a congenital hereditary condition caused by a dominant autosomal mu...
The cleidocranial dysplasia is a rare disease which can occur either spontaneously or by a dominant ...
Cleidocranial Dysplasia (CCD) is a rare autosomal dominant syndrome that occurs in approximate...
Cleidocranial dysplasia (CCD) is a rare syndrome usually caused by an autosomal dominant gene, altho...
Abstract Background Cleidocranial dysplasia (CCD) is a rare congenital autosomal dominant skeletal d...
Background: Cleidocranial dysplasia (CCD) is a rare inherited skeletal dysplasia, with an incidence ...
Introduction: Cleidocranial dysplasia (CCD) is an autosomal dominant disorder primarily affecting bo...
Cleidocranial dysplasia (CCD) is an autosomal dominant disease with a wide range of expression, char...
Cleidocranial dysplasia (CCD) is a rare disorder which is inherited as an autosomal genetic trait. I...
Introduction. Cleidocranial dysplasia (CCD) is an inherited disease caused by mutations in the RUNX2...
Patients with cleidocranial dysplasia commonly present with significant dental problems such as rete...
Cleidocranial dysplasia (CCD) is a rare autosomal dominant skeletal disease, which is caused by muta...
Introduction: Cleido-cranial dysplasia (CCD) is a rare congenital disorder with an autosomal dominan...
Cleidocranial dysplasia (Dysostosis) is an autosomal dominant disease with a wide range of expressio...
Cleidocranial dysplasia (CCD) is a congenital autosomal dominant syndrome characterised by dental an...
Cleidocranial dysplasia (CCD) is a congenital hereditary condition caused by a dominant autosomal mu...
The cleidocranial dysplasia is a rare disease which can occur either spontaneously or by a dominant ...
Cleidocranial Dysplasia (CCD) is a rare autosomal dominant syndrome that occurs in approximate...
Cleidocranial dysplasia (CCD) is a rare syndrome usually caused by an autosomal dominant gene, altho...
Abstract Background Cleidocranial dysplasia (CCD) is a rare congenital autosomal dominant skeletal d...
Background: Cleidocranial dysplasia (CCD) is a rare inherited skeletal dysplasia, with an incidence ...
Introduction: Cleidocranial dysplasia (CCD) is an autosomal dominant disorder primarily affecting bo...
Cleidocranial dysplasia (CCD) is an autosomal dominant disease with a wide range of expression, char...
Cleidocranial dysplasia (CCD) is a rare disorder which is inherited as an autosomal genetic trait. I...
Introduction. Cleidocranial dysplasia (CCD) is an inherited disease caused by mutations in the RUNX2...
Patients with cleidocranial dysplasia commonly present with significant dental problems such as rete...
Cleidocranial dysplasia (CCD) is a rare autosomal dominant skeletal disease, which is caused by muta...
Introduction: Cleido-cranial dysplasia (CCD) is a rare congenital disorder with an autosomal dominan...
Cleidocranial dysplasia (Dysostosis) is an autosomal dominant disease with a wide range of expressio...
Cleidocranial dysplasia (CCD) is a congenital autosomal dominant syndrome characterised by dental an...
Cleidocranial dysplasia (CCD) is a congenital hereditary condition caused by a dominant autosomal mu...
The cleidocranial dysplasia is a rare disease which can occur either spontaneously or by a dominant ...