Results 51 to 60 of about 2,769 (118)
Denosumab treatment for fibrous dysplasia [PDF]
Fibrous dysplasia (FD) is a skeletal disease caused by somatic activating mutations of the cyclic adenosine monophosphate (cAMP)‐regulating protein, α‐subunit of the Gs stimulatory protein (G s α).
Albright +41 more
core +1 more source
Radiographic classification of coronal plane femoral deformities in polyostotic fibrous dysplasia [PDF]
Fibrous dysplasia of bone is a skeletal dysplasia with a propensity to affect the femur in its polyostotic form, leading to deformity, fracture, and pain.
Boyce, A +5 more
core +1 more source
Maxillary fibrous dysplasia associated with McCune-Albright syndrome. A case study
McCune Albright syndrome (MCA) is a rare complication of genetic origin. The authors present a case study of a patient with MCA diagnosed with multifocal fibrous dysplasia in his limb and craniofacial bones.
Wójcik Sylwia +4 more
doaj +1 more source
Jaffe Lichtenstein Type Polyostotic Fibrous Dysplasia with Unilateral Absent Testis [PDF]
Fibrous dysplasias are developmental bone disorders in which the medullary cavity is replaced by fibrous tissue. It can be monostotic involving a single bone or polyostotic involving multiple bones.
Anand Ramakrishnan +3 more
doaj +1 more source
A rare case of McCune Albright syndrome [PDF]
McCune Albright syndrome is characterized by the clinical triad of precocious puberty, polyostotic fibrous dysplasia, and café-au-lait pigmentation. Authors reported the case of a 6 years old girl presenting with vaginal bleeding.
Banga, Siftie-Kaur, Patil, Pooja
core +2 more sources
Cardiac events are rare, easily neglected, but potentially fatal complications of McCune–Albright syndrome. An 18‐year‐old woman underwent proximal femur osteotomy and intramedullary nail fixation for correction of shepherd's crook deformity at our ...
Rongjie Wu, Guangtao Fu
doaj +1 more source
Introduction McCune-Albright syndrome is a complex inborn disorder due to early embryonal postzygotic somatic activating mutations in the GNAS1 gene. The phenotype is very heterogeneous and includes polyostotic fibrous dysplasia, typically involving the ...
Classen Carl +4 more
doaj +1 more source
The paradox of cancer genes in non-malignant conditions: implications for precision medicine. [PDF]
Next-generation sequencing has enabled patient selection for targeted drugs, some of which have shown remarkable efficacy in cancers that have the cognate molecular signatures.
Adashek, Jacob J +3 more
core
McCune–Albright syndrome is a disorder of fibrous bone dysplasia complicated by skin pigmentation and endocrine abnormalities. Although temporal bone lesions are rare, surgical treatment is required when external auditory canal (EAC) stenosis develops ...
Takaomi Kurioka +5 more
doaj +1 more source
A Case of Atypical McCune-Albright Syndrome with Vaginal Bleeding [PDF]
Background: McCune-Albright syndrome (MAS) is a rare non-inherited disorder characterized by the clinical triad of precocious puberty, cafe-au-lait skin lesions, and fibrous dysplasia of bone.
Hashemipour, M. +4 more
core +1 more source

