Apert Syndrome: New treatment and a perspective for the future

Autor:	Hiroê Alencar Braga, Janaina Batista Pereira, Cícera Janielly de Matos Cassiano, Kécia Silva Damasceno, Vânia Barbosa do Nascimento, Patrícia Gonçalves Pinheiro, Bruno Gonçalves Leite, Ana Beatriz Tavares Filgueiras, Hellen Lúcia Caldas Lins, Modesto Leite Rolim Neto
Rok vydání:	2015
Předmět:	musculoskeletal diseases congenital hereditary and neonatal diseases and abnormalities Pediatrics medicine.medical_specialty Polydactyly business.industry Perspective (graphical) medicine General Medicine Apert syndrome medicine.disease business Craniosynostosis
Zdroj:	International Archives of Medicine.
ISSN:	1755-7682
DOI:	10.3823/1686
Popis:	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.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::062b9042e09a465f7fee34fa90091317 https://doi.org/10.3823/1686 Zobrazit plný text záznamu