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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Shranjeno v:
Bibliografske podrobnosti
izdano v:Case Rep Dent
Main Authors: 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
Format: Artigo
Jezik:Inglês
Izdano: Hindawi Publishing Corporation 2016
Teme:
Case Report
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC4960323/
https://ncbi.nlm.nih.gov/pubmed/27478655
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2016/9685429
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