OROFACIAL FINDINGS IN NOONAN SYNDROME: A CASE REPORT

Authors: Raluca Maria Mocanu, Irina Nicoleta Zetu , Carmen Vulpoiu, Adriana Balan

Abstract:

Noonan syndrome is an autosomal dominant multisystem disorder, associated with cardiac anomalies and a distinctive facial appearance, characterized by genetic heterogeneity. Noonan syndrome affects both females and males, and has an estimated incidence of 1 per 1,000‑2,500 live births. The present report aims at presenting the cranio‑dento‑facial findings in a case of Noonan syndrome in a 6 year‑old male.