Diagnosis of Cleidocranial Dysplasia in Routine Chest Radiograph
نویسندگان
چکیده
منابع مشابه
Cleidocranial dysplasia
Cleidocranial dysplasia (CCD) is an autosomal dominant disorder resulting in the skeletal and dental abnormalities due to the disturbance in ossification of the bones. Clavicle is the most commonly affected bone. The prevalence of CCD is one in millions of live births. In this report, we present a case of 10-years-old boy showing features of this condition.
متن کاملAbnormal pulmonary density discovered on routine chest radiograph.
Figure 4. Enhanced CT image of the liver shows enlargement of the hepatic artery (arrows). Innumerable small, irregular vascular liver lesions are again seen (arrowheads). Figure 1. Posteroanterior radiograph of the chest demonstrates an abnormal density (arrows) in the inferior portion of the left lung. Figure 2. Computed tomography (CT) of the chest (lung window) shows a lobulated mass (arrow...
متن کاملFamilial Cleidocranial Dysplasia
Cleidocranial dysplasia or mutational dysostosis or cleidocranial dysostosis is a generalized skeletodental dysplastic disorder, inherited in an autosomal dominant pattern. The expression of this disorder can vary widely in severity, even within the same family. This is a relatively rare disease and has no standard effective treatment option as of yet. Here we present a case report of affected ...
متن کاملRUNX2 mutations in cleidocranial dysplasia.
The runt-related transcription factor 2 gene (RUNX2), which is also known as CBFA1, is a master regulatory gene in bone formation. Mutations in RUNX2 have been identified in cleidocranial dysplasia (CCD) patients. CCD is a rare autosomal dominant skeletal dysplasia that is characterized by delayed closure of cranial sutures, aplastic or hypoplastic clavicle formation, short stature, and dental ...
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...
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ژورنال
عنوان ژورنال: Circulation
سال: 2007
ISSN: 0009-7322,1524-4539
DOI: 10.1161/circulationaha.107.699769