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Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Osteochondrodysplasias > Fibrous Dysplasia of Bone > Fibrous Dysplasia, Polyostotic
... > Musculoskeletal Diseases > Bone Diseases > Bone Diseases, Developmental > Osteochondrodysplasias > Fibrous Dysplasia of Bone > Fibrous Dysplasia, Polyostotic

Preferred term

Fibrous Dysplasia, Polyostotic  

Type

  • Topical Descriptor

Broader concept

Entry terms

  • Polyostotic Fibrous Dysplasia

Note

  • sometimes Jaffe-Lichtenstein (usually monostotic) goes here: check text; craniofacial fibrous dysplasia: coord IM with FACIAL BONES (IM) + SKULL (IM)

Scope note

  • FIBROUS DYSPLASIA OF BONE affecting several bones. When melanotic pigmentation (CAFE-AU-LAIT SPOTS) and multiple endocrine hyperfunction are additionally associated it is referred to as Albright syndrome.

History note

  • 91(75); was see under FIBROUS DYSPLASIA OF BONE 1967-90; ALBRIGHT'S DISEASE & JAFFE-LICHTENSTEIN DISEASE were see under OSTEITIS FIBROSA 1963-66

In other languages

  • polyosteoottinen fibroottinen dysplasia

    Finnish

  • Albright-McCune-Sternberg
  • Albright-McCune-Sternbergin oireyhtymä
  • Albright-McCune-Sternbergin syndrooma
  • Albright(-McCune)(-Sternbergin) oireyhtymä
  • dysplasia fibrosa polyostotica
  • dysplasia polyostotica fibrotica
  • polyostoottinen fibroottinen dysplasia
  • syndroma Albright(-McCune)(-Sternberg)
  • usean luun fibroottinen dysplasia
  • Fibrös dysplasi, polyostotisk

    Swedish

URI

http://www.yso.fi/onto/mesh/D005359

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