Authors
Abstract
Introduction: Congenital arhinia is a very rare anomalia which can be observed total or partial arhinia. We assessed a case which is affected to congenital arhinia, its reasons and signs in the present study.
Case report: The patient is a 41w neonate who is affected to congenital arhinia, hypertelorism, cleft lip and palate. There was just a significant note in neonatal history of family which showed their first child was affected to anomalia. The neonate was transferred to a well-equip center for doing more assessments. At the present time, general condition of the neonate is good.
Conclusion: Congenital arhinia is a very rare anomaly with an unknown etiology. This anomaly may be associated with the other medline anomalies.
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