Case Report: Rare Presentation of Dentin Abnormalities in Loeys-Dietz Syndrome Type I

• Główni autorzy: Priyam Jani (Autor), Olivier Duverger (Autor), Rashmi Mishra (Autor), Pamela A. Frischmeyer-Guerrerio (Autor), Janice S. Lee (Autor)
• Format: Książka
• Wydane: Frontiers Media S.A., 2021-08-01T00:00:00Z.
• Hasła przedmiotowe: article
• Dostęp online: Connect to this object online.

Loeys-Dietz syndrome type 1 (LDS1) is caused by a mutation in the transforming growth factor-beta receptor 1 (TGFBR1) gene. We previously characterized the oral and dental anomalies in a cohort of individuals diagnosed with LDS and showed that LDS1 had a high frequency of oral manifestations, and mo...