Cargando…
The clinical manifestations, molecular mechanisms and treatment of craniosynostosis
Craniosynostosis is a major congenital craniofacial disorder characterized by the premature fusion of cranial suture(s). Patients with severe craniosynostosis often have impairments in hearing, vision, intracranial pressure and/or neurocognitive functions. Craniosynostosis can result from mutations,...
Autores principales: | Stanton, Eloise, Urata, Mark, Chen, Jian-Fu, Chai, Yang |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9044212/ https://www.ncbi.nlm.nih.gov/pubmed/35451466 http://dx.doi.org/10.1242/dmm.049390 |
Ejemplares similares
-
Neuro-Ophthalmological Manifestations of Craniosynostosis: Current Perspectives
por: Duan, Michael, et al.
Publicado: (2021) -
Craniosynostosis Secondary to Rickets: Manifestations on Computed Tomography
por: Wang, Page I., et al.
Publicado: (2015) -
Signaling Mechanisms Underlying Genetic Pathophysiology of Craniosynostosis
por: Wu, Xiaowei, et al.
Publicado: (2019) -
Multidisciplinary care of craniosynostosis
por: Buchanan, Edward P, et al.
Publicado: (2017) -
Signaling mechanisms implicated in cranial sutures pathophysiology: Craniosynostosis
por: Katsianou, Maria A., et al.
Publicado: (2016)