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Novel GNAI3 mutation in a Chinese auriculocondylar syndrome family and treatment of severe dentofacial deformities: A 5-years follow-up case report

2024-04-10

Abstract excerpt

<title>Abstract</title> <p>Background Auriculocondylar syndrome (ARCND) is an extremely rare autosomal dominant or recessive condition and the typical triad manifestations of ARCND are question mark ears (QMEs), mandibular condyle hypoplasia, and micrognathia. This severe dental and maxillofacial malformations have caused great trouble to patient’s life and clinical treatment. Now only a few ARCND cases are repo...

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Literature Corpus work: 31a482d6-b757-5c6e-80e9-c63b9de40155
DOI: 10.21203/rs.3.rs-4160232/v1

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