Nuevas manifestaciones orales del síndrome branquio-óculo-facial. Caso clínico

Translated title of the contribution: New oral manifestations of branchio-oculo-facial syndrome. Case report

Juan B. García Flores, César E. Escamilla Ocañas, Héctor R. Martínez Menchaca, Ma Guadalupe Treviño Alanís, Gerardo Rivera Silva

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)


The branchio-oculo-facial syndrome is a dominant autosomic condition with variable expressivity that affects particularly the facial and neck structures by an inadequate development of the first and second branchial arch. It is characterized by malformations of eyes and ears, with distinct facial characteristics. It is associated with alterations in TFAP2A gene. We present a patient with 9 years of age with phenotype of the branchio-oculo-facial syndrome and the presence of 2 new oral manifestations, the bifid uvula and the tongue with partial central cleft, not yet described in this clinical condition.

Translated title of the contributionNew oral manifestations of branchio-oculo-facial syndrome. Case report
Original languageSpanish
Pages (from-to)e14-e16
Number of pages3
JournalArchivos Argentinos de Pediatria
Issue number1
Publication statusPublished - 1 Jan 2015

All Science Journal Classification (ASJC) codes

  • Pediatrics, Perinatology, and Child Health


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