Cleidocranial dysplasia: description with emphasis on the radiographic aspects of three cases in a family

We describe three cases of cleidoclavicular dysplasia in a family, a rare genetic syndrome, presenting autosomal dominant behavior, but with 20-40% of sporadic cases, with an estimated incidence of 1-9/ 1.000.000. The study is based on a family consisting of the parent couple, two daughters and one...

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Hauptverfasser:	Rodolfo Mendes Queiroz, José Eduardo Martins Coelho, Leandro Fuso Ruiz, Rodrigo Castro Cervato, Mariana do Val Cervelatti, Michela Prestes Gomes, Marcos Pontes Muniz
Format:	Artigo
Sprache:	Português
Veröffentlicht:	Universidade de São Paulo 2018-05-01
Schriftenreihe:	Medicina
Schlagworte:	Cleidocranial Dysplasia. Wormians. Hyperdontia. Syndrome.
Online-Zugang:	http://www.revistas.usp.br/rmrp/article/view/146414
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