"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.
- Camurati-Engelmann Syndrome
- Camurati Engelmann Syndrome
- Camurati-Engelmann Disease
- Camurati Engelmann Disease
- Engelmann's Disease
- Diaphyseal Dysplasia, Progressive
- Diaphyseal Dysplasias, Progressive
- Dysplasia, Progressive Diaphyseal
- Dysplasias, Progressive Diaphyseal
- Engelmann Disease
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 the URMC Research Network by year, and whether "Camurati-Engelmann Syndrome" was a major or minor topic of these publication.