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Concept information

Terme préférentiel

Exostoses, Multiple Hereditary  

Type

  • mesh:Descriptor

Définition

  • Hereditary disorder transmitted by an autosomal dominant gene and characterized by multiple exostoses (multiple osteochondromas) near the ends of long bones. The genetic abnormality results in a defect in the osteoclastic activity at the metaphyseal ends of the bone during the remodeling process in childhood or early adolescence. The metaphyses develop benign, bony outgrowths often capped by cartilage. A small number undergo neoplastic transformation.

Synonyme(s)

  • Bessel-Hagen Disease
  • Chondrodysplasia, Hereditary Deforming
  • Diaphyseal Aclasis
  • Exostoses, Familial
  • Exostoses, Hereditary Multiple
  • Exostoses, Multiple
  • Exostoses, Multiple Cartilaginous
  • Exostoses, Multiple, Type I
  • Exostosis, Familial
  • Exostosis, Hereditary Multiple
  • Exostosis, Multiple
  • Exostosis, Multiple Cartilaginous
  • Familial Exostoses
  • Hereditary Multiple Exostoses
  • Hereditary Multiple Exostosis
  • Multiple Cartilaginous Exostoses
  • Multiple Hereditary Exostoses
  • Multiple Osteochondromas
  • Multiple Osteochondromatosis
  • Osteochondromas, Multiple

Traductions

  • français

  • Aclasie diaphysaire
  • Chondrodysplasie déformante héréditaire
  • Chondrodysplasie héréditaire déformante
  • Maladie de Bessel-Hagen
  • Maladie exostosante multiple
  • Maladie ostéogénique
  • Ostéochondromatose diffuse de Bessel-Hagen
  • Ostéochondromes multiples

URI

http://data.loterre.fr/ark:/67375/JVR-WPXK4HP3-Q

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RDF/XML TURTLE JSON-LD Date de création 01/01/1999, dernière modification le 08/07/2013