Structured Summary
Abstract
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.
MeSH Record
Classification
Broader headings
Related Concepts
Knowledge Graph
Drag nodes to rearrange; hover to trace links; click a node to open its page.
MeSH Record
Synonyms
15 entry terms
- Camurati-Engelmann Disease
- Diaphyseal Dysplasia 1, Progressive
- Diaphyseal Dysplasia, Progressive
- Diaphyseal Hyperostosis
- Engelmann Disease
- Engelmann's Disease
- Progressive Diaphyseal Dysplasia
- Camurati Engelmann Disease
- Camurati Engelmann Syndrome
- Diaphyseal Dysplasias, Progressive
- Diaphyseal Hyperostoses
- Dysplasia, Progressive Diaphyseal
- Dysplasias, Progressive Diaphyseal
- Hyperostoses, Diaphyseal
- Hyperostosis, Diaphyseal
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
2007(1975)
MeSH Hierarchy
Tree Numbers
AMA Style
References
- National Library of Medicine. Camurati-Engelmann Syndrome. Medical Subject Headings (MeSH). 2026. Unique ID D003966. http://id.nlm.nih.gov/mesh/2026/D003966
- Camurati-Engelmann Syndrome. In: Wikipedia. https://en.wikipedia.org/wiki/Camurati%E2%80%93Engelmann_disease
- Camurati-Engelmann Syndrome. In: Wikidata. https://www.wikidata.org/wiki/Q498487