Results 161 to 170 of about 3,948 (205)

Cleidocranial dysplasia - A case report

open access: yesJournal of Orofacial Sciences, 2011
Gautam Srivastava   +5 more
doaj  

Bone Morphogenetic Proteins: An Update on Basic Biology and Clinical Relevance

open access: yes, 1999
Amedee   +122 more
core   +1 more source

Molecular Genetics of Cleidocranial Dysplasia

Fetal and Pediatric Pathology, 2020
Cleidocranial 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
openaire   +2 more sources

Cleidocranial Dysplasia

Journal of Orofacial Research, 2012
Sunanda Chavva   +3 more
  +5 more sources

Cleidocranial dysplasia. Case report

Australian Dental Journal, 1995
AbstractA 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
openaire   +2 more sources

Cleidocranial Dysplasia

Applied Radiology, 2022
Neha Boski, Rohan Raj
openaire   +1 more source

Bone Scintigraphy in Cleidocranial Dysplasia

Clinical Nuclear Medicine, 2004
Cleidocranial 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
openaire   +3 more sources

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