Identification of a Novel <i>FAM83H</i> Mutation and Management of Hypocalcified Amelogenesis Imperfecta in Early Childhood

Identification of a Novel <i>FAM83H</i> Mutation and Management of Hypocalcified Amelogenesis Imperfecta in Early Childhood

Amelogenesis imperfecta (AI) is a heterogeneous group of rare genetic disorders affecting amelogenesis during dental development. Therefore, the molecular genetic etiology of AI can provide information about the nature and progress of the disease. To confirm the genetic etiology of AI in a Korean fa...

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Bibliographic Details
Main Authors: Ji-Soo Song, Yejin Lee, Teo Jeon Shin, Hong-Keun Hyun, Young-Jae Kim, Jung-Wook Kim
Format: Article
Language:English
Published: MDPI AG 2022-03-01
Series:Children
Subjects:
amelogenesis imperfecta
hypocalcified
general anesthesia
stainless steel crown
zirconia crown
<i>FAM83H</i>
Online Access:https://www.mdpi.com/2227-9067/9/3/429

Internet

https://www.mdpi.com/2227-9067/9/3/429

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