Maxillofacial Changes in Melnick-Needles Syndrome

Background. Melnick-Needles Syndrome is rare congenital hereditary skeletal dysplasia caused by mutations in the FLNA gene, which codifies the protein filamin A. This condition leads to serious skeletal abnormalities, including the stomatognathic region. Case Presentation. This paper describes the c...

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Detalles Bibliográficos
Autores principales: Albuquerque do Nascimento, Leilane Larissa, Salgueiro, Monica da Consolação Canuto, Quintela, Mariana, Teixeira, Victor Perez, Mota, Ana Carolina Costa, de Godoy, Camila Haddad Leal, Bussadori, Sandra Kalil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4960323/
https://www.ncbi.nlm.nih.gov/pubmed/27478655
http://dx.doi.org/10.1155/2016/9685429

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4960323/
https://www.ncbi.nlm.nih.gov/pubmed/27478655
http://dx.doi.org/10.1155/2016/9685429

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