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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Sparad:
Bibliografiska uppgifter
I publikationen:Case Rep Dent
Huvudupphovsmän: 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
Materialtyp: Artigo
Språk:Inglês
Publicerad: Hindawi Publishing Corporation 2016
Ämnen:
Case Report
Länkar: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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