| Literature DB >> 23906991 |
A Schindler1, L Guazzarotti, C Mameli, E Urbani, F Mozzanica, L Guerrini, G V Zuccotti.
Abstract
The congenital vomer defect (CVD) is a rare and still partially unknown condition. Only few cases have been reported in the international literature and the large majority of them appeared to be isolated. We report a case of CVD detected in a 7-year-old girl affected by ectodermal dysplasia clefting syndrome caused by a mutation of the TP63 gene.Entities:
Keywords: Clefting; EEC; Nasal septum; Ossification; P63 gene; Vomeral bone
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Year: 2013 PMID： 23906991 DOI： 10.1016/j.ijporl.2013.06.027
Source DB: PubMed Journal: Int J Pediatr Otorhinolaryngol ISSN： 0165-5876 Impact factor: 1.675