Article
Single median maxillary central incisor syndrome and variant in SMO gene associated with SHH pathway.
International journal of pediatric otorhinolaryngology - 1 Jul 2020
Zatoński Tomasz, Pazdro-Zastawny Katarzyna, Morawska-Kochman Monika, Biela Mateusz, Kołtowska Anna, Rydzanicz Małgorzata, Rozensztrauch Anna, Kosińska Joanna, Dorobisz Karolina, Płoski Rafał, Śmigiel Robert
Abstract excerpt
Solitary median maxillary central incisor syndrome (SMMCI) is a rare congenital oronasal-dental midline anomaly. The aim of this paper is a presentation of a patient with SMMCI without other visible dentofacial anomalies, with a potentially new molecular etiology consisting of a gene-gene reaction and conservative therapeutic approach to nasal obstruction. Potentially pathogenic variants in the SMO gene...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.