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

• Main Authors: Yulin Shi (Author), Liang Rong (Author), Siying Liu (Author), Yiwen Liu (Author), Chunlin Zong (Author), Jinbiao Lu (Author), Hongtao Shang (Author), Yang Xue (Author), Lei Tian (Author)
• Format: Book
• Published: BMC, 2024-07-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Abstract Background Auriculocondylar syndrome (ARCND) is an extremely rare autosomal dominant or recessive condition that typically manifests as question mark ears (QMEs), mandibular condyle hypoplasia, and micrognathia. Severe dental and maxillofacial malformations present considerable challenges i...