Broad Spectrum of Skeletal Malformation Complex in Patients with Cleidocranial Dysplasia Syndrome: Radiographic and Tomographic Study
نویسندگان
چکیده
منابع مشابه
Broad Spectrum of Skeletal Malformation Complex in Patients with Cleidocranial Dysplasia Syndrome: Radiographic and Tomographic Study
PURPOSE Cleidocranial dysplasia is an autosomal dominant disorder characterized by defective ossification of the intramembraneous ossification (primarily the clavicles, cranium, and pelvis), and it is caused by mutations in the RUNX2 gene that is responsible for osteoblast differentiation. Spine deformities were of progressive nature and considered to be the major orthopedic abnormalities encou...
متن کاملCleidocranial Dysplasia: A Clinico-radiographic Spectrum with Differential Diagnosis
INTRODUCTION Cleidocranial dysplasia (CCD) is characterized by aplasia or hypoplasia of the clavicles, characteristic craniofacial malformations, and the presence of numerous supernumerary and unerupted teeth. It affects bones derived from both intra-membranous and endochondral ossification. Incidence has been reported as 1 in 10,00,000. It is caused by mutation in the gene encoding transcripti...
متن کاملSkeletal and Dental Features of Cleidocranial Dysplasia
1 Department of Oral Medicine and Radiology, A B Shetty Memorial Institute of Dental Sciences Nitte University, Deralakatte, Mangalore-575 018, Karnataka, India. 2 MAHE Institute of Dental Sciences and Hospital, Chalakkara, Pallor, Manipal University, Manipal, Karnataka, India. 3 Department of Periodontics, A B Shetty Memorial Institute of Dental Sciences, Nitte University, Deralakatte, Mangalo...
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Background and purpose: Temporomandibular joint (TMJ) disorders are abnormalities that interfere with the shape or normal functioning of the joint, characterized by a group of clinical symptoms including pain, joint sounds, and limitation or deviation when opening the mouth. Considering the effect of skeletal relationships of the jaw on the shape, size, and morphologic variations of the condyle...
متن کاملEhlers-Danlos syndrome versus cleidocranial dysplasia
Dear Sir, The early identification of hereditary syndromes is essential for planning medical and surgical interventions for reducing the risk of complications [1]. Unfortunately, clinical phenotypes of hereditary syndromes in the first years of life and in mild cases are often poorly characterized. Some disease symptoms are also common to several different genetic conditions. Cleidocranial dysp...
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ژورنال
عنوان ژورنال: Clinical Medicine Insights: Arthritis and Musculoskeletal Disorders
سال: 2013
ISSN: 1179-5441,1179-5441
DOI: 10.4137/cmamd.s11933