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Cleidocranial dysplasia - A case report
Gautam Srivastava +5 more
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Bone Morphogenetic Proteins: An Update on Basic Biology and Clinical Relevance
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Molecular Genetics of Cleidocranial Dysplasia
Fetal and Pediatric Pathology, 2020Cleidocranial dysplasia (CCD) is a genetic disorder with an autosomal dominant inheritance pattern. CCD characterized by abnormal clavicles, patent sutures and fontenelles, supernumerary teeth and short stature. Approximately 60-70% of CCD patients have mutations in the RUNX2 gene.
Jamshid Motaei +9 more
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Cleidocranial dysplasia. Case report
Australian Dental Journal, 1995AbstractA 29‐year‐old Caucasian woman who presented with short stature and multiple unerupted supernumerary teeth is described. Radiological investigations of her cranial and skeletal abnormalities revealed cleidocranial dysplasia. Because of the advanced age of the patient and contraindication for orthodontic treatment, only surgical and prosthetic ...
F, Taşar +4 more
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Bone Scintigraphy in Cleidocranial Dysplasia
Clinical Nuclear Medicine, 2004Cleidocranial dysplasia (CLCD) is an autosomal-dominant disorder. There is altered bone formation with clavicular hypoplasia or agenesis with a narrow thorax, causing approximation of the shoulders in front of the chest occurring with delayed ossification of the skull, excessively large fontanelles, and delayed closure of the sutures.
Alper, Fatih +7 more
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