 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
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| 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
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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 |
|---|
| 2011 | 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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Uetsuka K, Suzuki T, Ogawa H, Sato H, Doi K, Nunoya T. A case of congenital hyperostosis in a newborn piglet. J Vet Med Sci. 2012 Feb; 74(2):259-62.
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Wergedal JE, Veskovic K, Hellan M, Nyght C, Balemans W, Libanati C, Vanhoenacker FM, Tan J, Baylink DJ, Van Hul W. Patients with Van Buchem disease, an osteosclerotic genetic disease, have elevated bone formation markers, higher bone density, and greater derived polar moment of inertia than normal. J Clin Endocrinol Metab. 2003 Dec; 88(12):5778-83.
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Borochowitz Z, Gozal D, Misselevitch I, Aunallah J, Boss JH. Familial Caffey's disease and late recurrence in a child. Clin Genet. 1991 Oct; 40(4):329-35.
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