 Fibrous Dysplasia, Polyostotic
"Fibrous Dysplasia, Polyostotic" 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.
FIBROUS DYSPLASIA OF BONE affecting several or many bones. When associated with melanotic pigmentation of the skin and endocrine disorders, it is known as Albright's syndrome. (From Dorland, 28th ed)
| Descriptor ID |
D005359
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| MeSH Number(s) |
C05.116.099.708.375.381
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| Concept/Terms |
Fibrous Dysplasia, Polyostotic- Fibrous Dysplasia, Polyostotic
- Dysplasia, Polyostotic Fibrous
- Dysplasias, Polyostotic Fibrous
- Fibrous Dysplasias, Polyostotic
- Polyostotic Fibrous Dysplasia
- Polyostotic Fibrous Dysplasias
Albright's Syndrome- Albright's Syndrome
- Albright Syndrome
- Albrights Syndrome
- Syndrome, Albright's
- McCune-Albright Syndrome
- McCune Albright Syndrome
- Syndrome, McCune-Albright
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Below are MeSH descriptors whose meaning is more general than "Fibrous Dysplasia, Polyostotic".
Below are MeSH descriptors whose meaning is more specific than "Fibrous Dysplasia, Polyostotic".
This graph shows the total number of publications written about "Fibrous Dysplasia, Polyostotic" by people in this website by year, and whether "Fibrous Dysplasia, Polyostotic" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1991 | 1 | 0 | 1 | | 1994 | 1 | 0 | 1 | | 1995 | 1 | 0 | 1 |
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Below are the most recent publications written about "Fibrous Dysplasia, Polyostotic" by people in Profiles.
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Dang D, Baig MN, Christoforidis G, Chiocca EA, Gabriel J. C2/C3 pathologic fractures from polyostotic fibrous dysplasia of the cervical spine treated with percutaneous vertebroplasty. Eur Spine J. 2007 Dec; 16 Suppl 3:250-4.
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Christoforidis G, Dang D, Gabriel J. Catheter-directed percutaneous transpedicular C2/C3 vertebroplasty in a patient with fibrous dysplasia using seldinger technique. AJNR Am J Neuroradiol. 2006 Sep; 27(8):1738-40.
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Phelan MC, Rogers RC, Clarkson KB, Bowyer FP, Levine MA, Estabrooks LL, Severson MC, Dobyns WB. Albright hereditary osteodystrophy and del(2) (q37.3) in four unrelated individuals. Am J Med Genet. 1995 Jul 31; 58(1):1-7.
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Gejman PV, Weinstein LS. Detection of mutations and polymorphisms of Gs alpha subunit gene by denaturing gradient gel electrophoresis. Methods Enzymol. 1994; 237:308-20.
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Weinstein LS, Shenker A, Gejman PV, Merino MJ, Friedman E, Spiegel AM. Activating mutations of the stimulatory G protein in the McCune-Albright syndrome. N Engl J Med. 1991 Dec 12; 325(24):1688-95.
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MacMAHON HE. The skeletal changes in Albright's disease. Am J Pathol. 1948 May; 24(3):682-4.
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