Cleft Palate in Apert Syndrome

Cleft Palate in Apert Syndrome

Apert syndrome is a rare genetic disorder characterized by craniosynostosis, midface retrusion, and limb anomalies. Cleft palate occurs in a subset of Apert syndrome patients. Although the genetic causes underlying Apert syndrome have been identified, the downstream signaling pathways and cellular m...

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Bibliographic Details
Main Authors: Delayna Willie, Greg Holmes, Ethylin Wang Jabs, Meng Wu
Format: Article
Language:English
Published: MDPI AG 2022-08-01
Series:Journal of Developmental Biology
Subjects:
Apert syndrome
cleft palate
FGF
FGFR2
high-arched palate
palatogenesis
Online Access:https://www.mdpi.com/2221-3759/10/3/33

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