 Hyperostosis, Cortical, Congenital
"Hyperostosis, Cortical, Congenital" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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)
| Descriptor ID |
D006958
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| MeSH Number(s) |
C05.116.099.708.479 C05.116.540.400 C16.614.465
|
| Concept/Terms |
Hyperostosis, Cortical, Congenital- Hyperostosis, Cortical, Congenital
- Congenital Hyperostosis, Cortical
- Congenital Hyperostoses, Cortical
- Cortical Congenital Hyperostoses
- Hyperostoses, Cortical Congenital
- Hyperostosis, Cortical Congenital
- Cortical Congenital Hyperostosis
- Familial Caffey's Disease
- Caffey's Disease, Familial
- Disease, Familial Caffey's
- Familial Caffey Disease
- Familial Caffeys Disease
- 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
- Caffey-De Toni-Silvermann Syndrome
- Caffey De Toni Silvermann Syndrome
- Syndrome, Caffey-De Toni-Silvermann
- Cortical Hyperostosis, Congenital
- Congenital Cortical Hyperostoses
- Congenital Cortical Hyperostosis
- Cortical Hyperostoses, Congenital
- Hyperostoses, Congenital Cortical
- Hyperostosis, Congenital Cortical
|
Below are MeSH descriptors whose meaning is more general than "Hyperostosis, Cortical, Congenital".
- Diseases [C]
- Musculoskeletal Diseases [C05]
- Bone Diseases [C05.116]
- Bone Diseases, Developmental [C05.116.099]
- Osteochondrodysplasias [C05.116.099.708]
- Hyperostosis, Cortical, Congenital [C05.116.099.708.479]
- Hyperostosis [C05.116.540]
- Hyperostosis, Cortical, Congenital [C05.116.540.400]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Infant, Newborn, Diseases [C16.614]
- Hyperostosis, Cortical, Congenital [C16.614.465]
Below are MeSH descriptors whose meaning is more specific than "Hyperostosis, Cortical, Congenital".
This graph shows the total number of publications written about "Hyperostosis, Cortical, Congenital" by people in this website by year, and whether "Hyperostosis, Cortical, Congenital" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2018 | 1 | 0 | 1 |
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Below are the most recent publications written about "Hyperostosis, Cortical, Congenital" by people in Profiles.
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Roberts MS, Burbelo PD, Egli-Spichtig D, Perwad F, Romero CJ, Ichikawa S, Farrow E, Econs MJ, Guthrie LC, Collins MT, Gafni RI. Autoimmune hyperphosphatemic tumoral calcinosis in a patient with FGF23 autoantibodies. J Clin Invest. 2018 12 03; 128(12):5368-5373.
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Wilson MP, Lindsley CB, Warady BA, Johnson JA. Hyperphosphatemia associated with cortical hyperostosis and tumoral calcinosis. J Pediatr. 1989 Jun; 114(6):1010-3.
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