Caffey Disease in Infancy: A diagnostic dilemma for primary care physicians

Caffey disease is a rare and self-limiting condition characterised by cortical hyperostosis with inflammation of adjacent fascia and muscles. It usually presents in infancy and clinical features include hyperirritability, acute inflammation with swelling of overlying soft tissues and subperiosteal n...

Descripción completa

Detalles Bibliográficos
Autores principales: Siddiqui, Shahid A., Siddiqui, Gulnaz F., Maurya, Manisha, Shrivastava, Anubha, Singh, Mukesh V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sultan Qaboos University Medical Journal, College of Medicine & Health Sciences 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7065700/
https://www.ncbi.nlm.nih.gov/pubmed/32190379
http://dx.doi.org/10.18295/squmj.2020.20.01.017

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7065700/
https://www.ncbi.nlm.nih.gov/pubmed/32190379
http://dx.doi.org/10.18295/squmj.2020.20.01.017

Ejemplares similares