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

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

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...

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Bibliographic Details
Main Authors: Priyam Jani, Olivier Duverger, Rashmi Mishra, Pamela A. Frischmeyer-Guerrerio, Janice S. Lee
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-08-01
Series:Frontiers in Dental Medicine
Subjects:
Loeys-Dietz syndrome
TGFBR1 mutation
TGF-beta signaling
dentin defect
dentinogenesis imperfecta
case report
Online Access:https://www.frontiersin.org/articles/10.3389/fdmed.2021.674136/full

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https://www.frontiersin.org/articles/10.3389/fdmed.2021.674136/full

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