We report an adult male patient born to normal and non-consanguineous
parents with midline craniofacial defects associated with branchial ar
ch anomalies. This combination of signs belongs to the oculoauriculofr
ontonasal spectrum. We compare our case with those previously reported
who had similar findings and discuss clinical aspects of the oculoaur
iculofrontonasal spectrum and frontofacionasal dysplasia.