Cleidocranial dysplasia (CCD) is an uncommon but well-known genetic skeletal condition. Several hundred affected persons are members of a large extended family in the Cape Town Mixed Ancestry community of South Africa. The clinical manifestations are often innocuous, but hyperdontia and other developmental abnormalities of the teeth are a major feature and may require special dental management. Over the past 40 years, the authors have encountered more than 100 affected persons in Cape Town. Emphasis has been on dental management, but medical, genetic, and social problems have also been addressed. In this article, we have reviewed the manifestations of the disorder in the light of our own experience, and performed a literature search w...
The cleidocranial dysplasia is a rare disease which can occur either spontaneously or by a dominant ...
Cleidocranial Dysplasia(CCD) is an autosomal dominant human bone disease characterized by abnormal c...
Cleidocranial dysplasia (CCD) is a congenital hereditary condition caused by a dominant autosomal mu...
Cleidocranial dysplasia (CCD) is an uncommon but well-known genetic skeletal condition. Several hund...
Introduction: Cleidocranial dysplasia (CCD) is an autosomal dominant disorder, also referred to ascl...
Cleidocranial dysplasia (CCD) is a rare disorder which is inherited as an autosomal genetic trait. I...
Cleidocranial dysplasia (CCD) is a rare disorder which is inherited as an autosomal genetic trait. I...
none3Cleidocranial dysplasia (CCD) is a rare disorder which is inherited as an autosomal genetic tra...
Cleidocranial dysplasia (CCD) is a bone disorder with cranial malformations, dental abnormaliti...
Cleidocranial Dysplasia (CCD) is a rare autosomal dominant syndrome that occurs in approximate...
Cleidocranial dysplasia (CCD) is an inherited autosomal dominant disorder affecting the skeletal and...
Aim: Cleidocranial dysostosis (CCD) is a rare congenital bone disorder with an autosomal dominant he...
Cleidocranial dysplasia (CCD) is a rare syndrome usually caused by an autosomal dominant gene, altho...
Aim: Cleidocranial dysostosis (CCD) is a rare congenital bone disorder with an autosomal dominant he...
none3AIM: Cleidocranial dysplasia (CCD) is a rare disorder that is inherited as an autosomal genetic...
The cleidocranial dysplasia is a rare disease which can occur either spontaneously or by a dominant ...
Cleidocranial Dysplasia(CCD) is an autosomal dominant human bone disease characterized by abnormal c...
Cleidocranial dysplasia (CCD) is a congenital hereditary condition caused by a dominant autosomal mu...
Cleidocranial dysplasia (CCD) is an uncommon but well-known genetic skeletal condition. Several hund...
Introduction: Cleidocranial dysplasia (CCD) is an autosomal dominant disorder, also referred to ascl...
Cleidocranial dysplasia (CCD) is a rare disorder which is inherited as an autosomal genetic trait. I...
Cleidocranial dysplasia (CCD) is a rare disorder which is inherited as an autosomal genetic trait. I...
none3Cleidocranial dysplasia (CCD) is a rare disorder which is inherited as an autosomal genetic tra...
Cleidocranial dysplasia (CCD) is a bone disorder with cranial malformations, dental abnormaliti...
Cleidocranial Dysplasia (CCD) is a rare autosomal dominant syndrome that occurs in approximate...
Cleidocranial dysplasia (CCD) is an inherited autosomal dominant disorder affecting the skeletal and...
Aim: Cleidocranial dysostosis (CCD) is a rare congenital bone disorder with an autosomal dominant he...
Cleidocranial dysplasia (CCD) is a rare syndrome usually caused by an autosomal dominant gene, altho...
Aim: Cleidocranial dysostosis (CCD) is a rare congenital bone disorder with an autosomal dominant he...
none3AIM: Cleidocranial dysplasia (CCD) is a rare disorder that is inherited as an autosomal genetic...
The cleidocranial dysplasia is a rare disease which can occur either spontaneously or by a dominant ...
Cleidocranial Dysplasia(CCD) is an autosomal dominant human bone disease characterized by abnormal c...
Cleidocranial dysplasia (CCD) is a congenital hereditary condition caused by a dominant autosomal mu...