OROFACIAL FEATURES IN GOLDENHAR SYNDROME

Goldenhar syndrome (GS) or hemifacial microsomia (OMIM #164210) is a rare genetic disorder related to gene 14q32, which involves defects in the 1st and 2nd branchial arches reflecting in craniofacial, cardiac, vertebral, and central nervous system alterations. The objective of this work was to demon...

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Bibliographic Details

Published in:	Oral surgery, oral medicine, oral pathology and oral radiology Vol. 134; no. 3; p. e114
Main Authors:	Santos, Catielma Nascimento, Araújo, Nathália Abdala, De Rezende, Nathalie Pepe Medeiros, Martins, Fabiana, Ortega, Karem López, Gallottini, Marina Helena Cury
Format:	Journal Article
Language:	English
Published:	Elsevier Inc 01-09-2022
Online Access:	Get full text
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