Craniosynostosis in Patients With X‐Linked Hypophosphatemia: A Review

Craniosynostosis is a rare condition of skull development, manifesting during fetal and early infant development, and is usually congenital. Craniosynostosis secondary to metabolic disorders, such as X‐linked hypophosphatemia (XLH), is less common and is typically diagnosed later than congenital cra...

Descripción completa

Detalles Bibliográficos
Autores principales: Munns, Craig F, Maguire, Edward P, Williams, Angela, Wood, Sue, Biggin, Andrew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10184010/
https://www.ncbi.nlm.nih.gov/pubmed/37197318
http://dx.doi.org/10.1002/jbm4.10728

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10184010/
https://www.ncbi.nlm.nih.gov/pubmed/37197318
http://dx.doi.org/10.1002/jbm4.10728

Ejemplares similares