Hyperostosis, Cortical, Congenital
A disease of young infants characterized by soft tissue swellings over the affected bones, fever, and irritability, and marked by periods of remission and exacerbation. (Dorland, 27th ed)
Year introduced: 1991
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Subheadings:
Tree Number(s): C05.116.099.708.479, C05.116.540.400, C16.614.465
MeSH Unique ID: D006958
Entry Terms:
- Caffey-De Toni-Silvermann Syndrome
- Caffey De Toni Silvermann Syndrome
- Syndrome, Caffey-De Toni-Silvermann
- Congenital Hyperostosis, Cortical
- Congenital Hyperostoses, Cortical
- Cortical Congenital Hyperostoses
- Hyperostoses, Cortical Congenital
- Hyperostosis, Cortical Congenital
- Cortical Congenital Hyperostosis
- Cortical Hyperostosis, Congenital
- Congenital Cortical Hyperostoses
- Congenital Cortical Hyperostosis
- Cortical Hyperostoses, Congenital
- Hyperostoses, Congenital Cortical
- Hyperostosis, Congenital Cortical
- Infantile Cortical Hyperostosis
- Cortical Hyperostoses, Infantile
- Cortical Hyperostosis, Infantile
- Hyperostoses, Infantile Cortical
- Hyperostosis, Infantile Cortical
- Infantile Cortical Hyperostoses
- Caffey Disease
- Disease, Caffey
- Familial Infantile Cortical Hyperostosis
- Familial Caffey's Disease
- Caffey's Disease, Familial
- Disease, Familial Caffey's
- Familial Caffey Disease
- Familial Caffeys Disease