Apert Syndrome: An Insight Into Dentofacial Features

Apert syndrome is a developmental malformation characterised by craniosynostosis (premature fusion of cranial sutures), midface hypoplasia, and syndactyly of hands and feet. Early synostosis of the coronal suture, cranial base, as well as agenesis of the sagittal suture, result in characteristic app...

Descripción completa

Detalles Bibliográficos
Autores principales: Jose, Bijimole, Emmatty, Tharian B, Methippara, John Joseph, Kumar, Kavita, Thampi, Nidhi Mary
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Medical Education
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8491803/
https://www.ncbi.nlm.nih.gov/pubmed/34659949
http://dx.doi.org/10.7759/cureus.17735

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8491803/
https://www.ncbi.nlm.nih.gov/pubmed/34659949
http://dx.doi.org/10.7759/cureus.17735

Ejemplares similares