Disostose cleidocraniana: Relato de dois casos familiares

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Cleidocranial dysostosis is a rare genetic syndrome with an autosomal dominant inheritance pattern. The most common manifestations include clavicular aplasia or hypoplasia, open fontanelles and abnormal dentition. The present report describes two familial cases whose late diagnosis was made by means of clinical and radiographic findings. The treatment was radical, with complete surgical teeth extraction and making of total dental prosthesis. © Colégio Brasileiro de Radiologia e Diagnóstico por Imagem.




Porciuncula, C. G. G., Lira, R. F. de, Soares, M. L. L., Araújo, D. L., Mota, L. R., & Lira, L. F. (2013). Disostose cleidocraniana: Relato de dois casos familiares. Radiologia Brasileira, 46(6), 382–384. https://doi.org/10.1590/S0100-39842013000600013

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