"Hyperostosis" 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.
Increase in the mass of bone per unit volume.
| Descriptor ID |
D015576
|
| MeSH Number(s) |
C05.116.540
|
| Concept/Terms |
Hyperostosis- Hyperostosis
- Hyperostoses
- Bone Hypertrophy
- Bone Hypertrophies
- Hypertrophies, Bone
- Hypertrophy, Bone
|
Below are MeSH descriptors whose meaning is more general than "Hyperostosis".
Below are MeSH descriptors whose meaning is more specific than "Hyperostosis".
This graph shows the total number of publications written about "Hyperostosis" by people in this website by year, and whether "Hyperostosis" 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 |
|---|
| 2013 | 0 | 1 | 1 |
| 2018 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Hyperostosis" by people in Profiles.
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Piard J, Lespinasse J, Vlckova M, Mensah MA, Iurian S, Simandlova M, Malikova M, Bartsch O, Rossi M, Lenoir M, Nugues F, Mundlos S, Kornak U, Stanier P, Sousa SB, Van Maldergem L. Cutis laxa and excessive bone growth due to de novo mutations in PTDSS1. Am J Med Genet A. 2018 03; 176(3):668-675.
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Sousa SB, Jenkins D, Chanudet E, Tasseva G, Ishida M, Anderson G, Docker J, Ryten M, Sa J, Saraiva JM, Barnicoat A, Scott R, Calder A, Wattanasirichaigoon D, Chrzanowska K, Simandlov? M, Van Maldergem L, Stanier P, Beales PL, Vance JE, Moore GE. Gain-of-function mutations in the phosphatidylserine synthase 1 (PTDSS1) gene cause Lenz-Majewski syndrome. Nat Genet. 2014 Jan; 46(1):70-6.
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Cataltepe O, Ekin Ozcan O, Sagmanli S, Onol B. A giant hyperostosing meningioma in a child. Neurochirurgia (Stuttg). 1992 Sep; 35(5):171-5.