 Camurati-Engelmann Syndrome
"Camurati-Engelmann Syndrome" 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.
An autosomal dominant form of dysplasia that is characterized by progressive thickening of diaphyseal cortex of long bones. Mutations in the gene that encodes TRANSFORMING GROWTH FACTOR BETA1 are one cause of this disorder.
| Descriptor ID |
D003966
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| MeSH Number(s) |
C05.116.099.708.180 C16.320.144
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| Concept/Terms |
Camurati-Engelmann Syndrome- Camurati-Engelmann Syndrome
- Camurati Engelmann Syndrome
- Progressive Diaphyseal Dysplasia
- Engelmann's Disease
- Camurati-Engelmann Disease
- Camurati Engelmann Disease
- Diaphyseal Dysplasia, Progressive
- Diaphyseal Dysplasias, Progressive
- Dysplasia, Progressive Diaphyseal
- Dysplasias, Progressive Diaphyseal
- Engelmann Disease
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Below are MeSH descriptors whose meaning is more general than "Camurati-Engelmann Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Camurati-Engelmann Syndrome".
This graph shows the total number of publications written about "Camurati-Engelmann Syndrome" by people in UAMS Profiles by year, and whether "Camurati-Engelmann Syndrome" was a major or minor topic of these publications.
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Below are the most recent publications written about "Camurati-Engelmann Syndrome" by people in Profiles over the past ten years.
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