Apert Syndrome: New treatment and a perspective for the future | Zendy

Bruno Gonçalves Leite | Zendy; Ana Beatriz Tavares Filgueiras | Zendy; Kécia Silva Damasceno | Zendy; Janaina Batista Pereira | Zendy; Vânia Barbosa do Nascimento | Zendy; Hiroê Alencar Braga | Zendy; Patrícia Gonçalves Pinheiro | Zendy; Hellen Lúcia Caldas Lins | Zendy; Modesto Leite Rolim Neto | Zendy; Cícera Janielly de Matos Cassiano | Zendy

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Apert Syndrome: New treatment and a perspective for the future

Author(s) -

Bruno Gonçalves Leite,

Ana Beatriz Tavares Filgueiras,

Kécia Silva Damasceno,

Janaina Batista Pereira,

Vânia Barbosa do Nascimento,

Hiroê Alencar Braga,

Patrícia Gonçalves Pinheiro,

Hellen Lúcia Caldas Lins,

Modesto Leite Rolim Neto,

Cícera Janielly de Matos Cassiano

Publication year - 2015

Publication title -

international archives of medicine

Language(s) - English

Resource type - Journals

ISSN - 1755-7682

DOI - 10.3823/1686

Subject(s) - apert syndrome , craniosynostosis , medicine , perspective (graphical) , craniosynostoses , polydactyly , dysostosis , pediatrics , surgery , anatomy , congenital disease , artificial intelligence , computer science

Treatment the Apert Syndrome is unique, therefore, divergences exist in the priority of the procedures performed by each team. The Apert Syndrome occurs in approximately 1/65,000 births and accounts for 4.5% of all craniosynostosis. Some changes in Apert Syndrome stand out, such as craniosynostosis and polydactyly.

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