Concept information
Término preferido
Camurati-Engelmann Syndrome
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Tipo
-
mesh:Descriptor
Definición
- 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.
Concepto genérico
Etiquetas alternativas
- Camurati-Engelmann Disease
- Diaphyseal Dysplasia 1, Progressive
- Diaphyseal Dysplasia, Progressive
- Diaphyseal Hyperostosis
- Engelmann Disease
- Engelmann's Disease
- Progressive Diaphyseal Dysplasia
En otras lenguas
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francés
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Dysplasie diaphysaire progressive
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Hyperostose diaphysaire
-
Maladie d'Engelmann
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Maladie de Camurati-Engelmann
URI
http://data.loterre.fr/ark:/67375/JVR-T6NMN5M3-B
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