Results 121 to 130 of about 1,796 (161)
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Development of the dentition in cleidocranial dysplasia
Journal of Oral Pathology and Medicine, 1990The purpose of the present investigation was to describe the formation, maturation and eruption of the dentition, including supernumerary teeth in a sample of patients with cleidocranial dysplasia. The dentition was evaluated from orthopantomograms, intraoral radiographs, cephalometric films, surgically removed teeth and intraoral photographs in 19 ...
Sven Kreiborg, B L Jensen
exaly +4 more sources
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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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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Newborn with cleidocranial dysplasia
Skeletal Radiology, 2022Franceschi, Roberto +4 more
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Cleidocranial dysplasia: Underdiagnosed and misdiagnosed?
The Indian Journal of Pediatrics, 1992Cleidocranial dysplasia (CCD) is a generalised disorder of bone ossification, the most obvious sites of involvement being the skull and the clavicles. Two patients ,are described in whom a variety of disorders were considered before the diagnosis was made on the basis of the radiological features.
L, Mehta, I C, Verma
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Cleidocranial Dysplasia in Mice
Annals of the New York Academy of Sciences, 1996S, Mundlos +3 more
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Somatic development in cleidocranial dysplasia
American Journal of Medical Genetics, 1990AbstractAs part of a more comprehensive investigation of general and craniofacial development in cleidocranial dysplasia (CCD), the present study describes general somatic development and analyzes longitudinal growth of 17 patients (seven males, ten females, aged 5–46 years) with CCD. Eleven were followed longitudinally.
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