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Concept information

Musculoskeletal Diseases > Joint Diseases > Osteoarthropathy, Primary Hypertrophic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Osteoarthropathy, Primary Hypertrophic
Musculoskeletal Diseases > Bone Diseases > Osteoarthropathy, Primary Hypertrophic

Preferred term

Osteoarthropathy, Primary Hypertrophic  

Type

  • mesh:Descriptor

Definition

  • A condition chiefly characterized by thickening of the skin of the head and distal extremities, deep folds and furrows of the skin of the forehead, cheeks, and scalp, SEBORRHEA; HYPERHIDROSIS; periostosis of the long bones, digital clubbing, and spadelike enlargement of the hands and feet. It is more prevalent in the male, and is usually first evident during adolescence. Inheritance is primarily autosomal recessive, but an autosomal dominant form exists.

Broader concept

Entry terms

  • Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive
  • Idiopathic Hypertrophic Osteoarthropathy
  • Pachydermoperiostosis
  • Pachydermoperiostosis, Autosomal Recessive
  • Touraine-Solente-Gole Syndrome

Allowable Qualifier(s)

In other languages

  • Pachydermopériostose

    French

  • Maladie de Touraine, Solente et Golé
  • Ostéoarthropathie hypertrophiante idiopathique
  • Ostéoarthropathie hypertrophiante primitive
  • Ostéoarthropathie hypertrophiante primitive autosomique récessive
  • Pachydermie plicaturée avec pachy-périostose de la face et des extrémités
  • Pachydermopériostose autosomique récessive
  • Syndrome de Touraine, Solente et Golé

URI

http://data.loterre.fr/ark:/67375/JVR-N4G0TQH1-N

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