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)
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 Harvard Catalyst Profiles by year, and whether "Hyperostosis, Cortical, Congenital" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
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1999 | 1 | 0 | 1 |
2005 | 1 | 0 | 1 |
Below are the most recent publications written about "Hyperostosis, Cortical, Congenital" by people in Profiles.
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Expanding the Phenotypic Spectrum of Kenny-Caffey Syndrome. J Clin Endocrinol Metab. 2023 08 18; 108(9):e754-e768.
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Topical Sodium Thiosulfate: A Treatment for Calcifications in Hyperphosphatemic Familial Tumoral Calcinosis? J Clin Endocrinol Metab. 2016 07; 101(7):2810-5.
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Caffey disease: new perspectives on old questions. Bone. 2014 Mar; 60:246-51.
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A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disorders. J Clin Invest. 2005 May; 115(5):1250-7.
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Radiologic case study. Infantile cortical hyperostosis (Caffey's disease). Orthopedics. 1999 Jul; 22(7):712, 707-8.