Evolution of a child with Treacher Collins syndrome undergoing physiotherapeutic treatment

• Κύριοι συγγραφείς: Bárbara Gabriela da S. Rodrigues (Συγγραφέας), Juliane Leonardo Oliveira Silva (Συγγραφέας), Pryscilla Gualberto Guimarães (Συγγραφέας), Cibelle Kayenne Martins Roberto Formiga (Συγγραφέας), Fabiana Pavan Viana (Συγγραφέας)
• Μορφή: Βιβλίο
• Έκδοση: Editora Champagnat.
• Θέματα: article
• Διαθέσιμο Online: Connect to this object online.

AbstractIntroduction Treacher Collins syndrome, or mandibulofacial dysostosis, is a hereditary disorder and is manifested by craniofacial malformations. The incidence is close to one case per 40,000 live births, without relation to gender or race. The infant carrier may present neurological developm...