Prenatal Diagnosis of Treacher-Collins Syndrome Using Three-Dimensional Ultrasonography and Differential Diagnosis with Other Acrofacial Dysostosis Syndromes

Treacher-Collins syndrome (TCS) is a rare dominant autosomal anomaly resulting from malformation or disruption of the development of the first and second branchial arches. It is characterized by micrognathia, malar hypoplasia, and malformations of the eyes and ears. The prenatal diagnosis using two-...

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Detalles Bibliográficos
Autores principales: Pereira, Daniela Cardoso, Bussamra, Luiz Claudio Silva, Araujo Júnior, Edward, Drummond, Carolina Leite, Nardozza, Luciano Marcondes Machado, Moron, Antonio Fernandes, Aldrighi, José Mendes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3638565/
https://www.ncbi.nlm.nih.gov/pubmed/23653874
http://dx.doi.org/10.1155/2013/203976

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3638565/
https://www.ncbi.nlm.nih.gov/pubmed/23653874
http://dx.doi.org/10.1155/2013/203976

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