INCIDENTAL FINDING OF CLEIDOCRANIAL DYSPLASIA IN AN ADOLESCENT WITH HEAD TRAUMA
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 کاملClassic case of cleidocranial dysplasia with an infected mandibular cyst
Introduction: Patients with cleidocranial dysplasia commonly present with significant dental problems, such as retention of multiple deciduous teeth, impaction or delayed eruption of teeth and the presence of multiple Madhu P. Sivan1, Jayakumar K.2, Jayalakshmi P. S.3, N. Sruthi4 Affiliations: 1MDS, Provisional Lecturer, Department of Oral and Maxillofacial Surgery, Government Medical College, ...
متن کامل"The lucky penny"--an incidental finding of hip dysplasia in a child with foreign body ingestion.
Undetected hip dysplasia can lead to significant morbidity. We report a case of development hip dysplasia, which was diagnosed incidentally following radiographic investigation for an ingested coin. CASE REPORT A two-year-old girl was brought to the emergency department following the ingestion of a one pence coin. A thoraco-abdominal radiograph demonstrated the presence of a coin within the fir...
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 ...
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ژورنال
عنوان ژورنال: Indian Journal of Child Health
سال: 2014
ISSN: 2349-6118,2349-6126
DOI: 10.32677/ijch.2014.v01.i02.014