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Descriptor English: Fibrous Dysplasia, Polyostotic
Descriptor Spanish: Displasia Fibrosa Poliostótica
Descriptor displasia fibrosa poliostótica
Entry term(s) síndrome de Albright
síndrome de McCune-Albright
Scope note: DISPLASIA FIBROSA ÓSEA que afecta a varios huesos. Cuando se asocia una pigmentación melanósica (MANCHAS CAFÉ CON LECHE) y múltiples hiperfunciones endocrinas, entonces hablamos de un síndrome de Albright.
Descriptor Portuguese: Displasia Fibrosa Poliostótica
Descriptor French: Dysplasie fibreuse polyostotique
Entry term(s): Albright Syndrome
Albright's Disease
Albright's Disease of Bone
Albright's Syndrome
Albright's Syndrome with Precocious Puberty
Albright-Mccune-Sternberg Syndrome
Albright-Sternberg Syndrome
Dysplasia, Polyostotic Fibrous
Dysplasias, Polyostotic Fibrous
Fibrous Dysplasia with Pigmentary Skin Changes and Precocious Puberty
Fibrous Dysplasias, Polyostotic
McCune Albright Syndrome
McCune-Albright Syndrome
Polyostotic Fibrous Dysplasia
Polyostotic Fibrous Dysplasias
Syndrome, Albright
Syndrome, Albright's
Syndrome, McCune-Albright
Tree number(s): C05.116.099.708.375.381
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D005359
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.
Annotation: sometimes Jaffe-Lichtenstein (usually monostotic) goes here: check text; craniofacial fibrous dysplasia: coord IM with FACIAL BONES (IM) + SKULL (IM)
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CN congenital
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Public MeSH Note: 91; was see under FIBROUS DYSPLASIA OF BONE 1967-90; ALBRIGHT'S DISEASE & JAFFE-LICHTENSTEIN DISEASE were see under OSTEITIS FIBROSA 1963-66
Online Note: use FIBROUS DYSPLASIA OF BONE to search FIBROUS DYSPLASIA, POLYOSTOTIC 1967-74; search ALBRIGHT'S DISEASE & JAFFE-LICHTENSTEIN DISEASE under OSTEITIS FIBROSA CYSTICA 1966
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
DeCS ID: 5494
Unique ID: D005359
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1991/01/01
Date of Entry: 1999/01/01
Revision Date: 2013/07/08
Fibrous Dysplasia, Polyostotic - Preferred
Concept UI M0008457
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.
Preferred term Fibrous Dysplasia, Polyostotic
Entry term(s) Dysplasia, Polyostotic Fibrous
Dysplasias, Polyostotic Fibrous
Fibrous Dysplasias, Polyostotic
Polyostotic Fibrous Dysplasia
Polyostotic Fibrous Dysplasias
Albright Syndrome - Narrower
Concept UI M0008458
Preferred term Albright Syndrome
Entry term(s) Albright's Disease
Albright's Disease of Bone
Albright's Syndrome
Albright's Syndrome with Precocious Puberty
Albright-Mccune-Sternberg Syndrome
Albright-Sternberg Syndrome
Fibrous Dysplasia with Pigmentary Skin Changes and Precocious Puberty
McCune Albright Syndrome
McCune-Albright Syndrome
Syndrome, Albright
Syndrome, Albright's
Syndrome, McCune-Albright



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