Results 61 to 70 of about 2,787 (193)
Introduction: Premature puberty, café-au-lait pigmentation, polyostotic fibrous dysplasia, and/or varied endocrine disorders make up the unusual condition known as McCune Albright Syndrome.
Mrinal Mahadev Kambli +5 more
doaj +1 more source
Monostotic fibrous dysplasia of the spine: report of a case involving a cervical vertebra [PDF]
Monostotic fibrous dysplasia of the spine is a rare entity. Only 26 cases, of which 11 were located in the cervical spine, are to be found in the literature.
Heini, P. +3 more
core
Post‐COVID‐19 Exacerbation of a Stable Fibrous Dysplasia: A Case Report
ABSTRACT Fibrous dysplasia (FD) is a rare, benign fibro‐osseous lesion characterized by replacement of normal bone with extensive fibrous stroma due to abnormalities in osteoblast differentiation. After puberty and during adulthood, FD lesions usually become quiescent. However, some cases show signs of regrowth and reactivation.
Mohammed Taib Fatih +7 more
wiley +1 more source
The use of hyperbaric oxygen therapy in actinomycotic osteomyelitis associated florid cemento osseous dysplasia: report of a familial case. [PDF]
Florid Cemento-Osseous Dysplasia (FCOD) is a well recognized fibro-osseous disease of the jaws commonly seen in the middle aged African women, although it may occur in the Caucasians and Asians.
Iyengar, Asha R. +3 more
core +1 more source
Skeletal Phenotype in Mulibrey Nanism, A Monogenic Skeletal Dysplasia With Fibrous Dysplasia
We present a cross‐sectional detailed radiographic evaluation of the skeletal phenotype in 33 patients, aged 4.5–48 years, with Mulibrey nanism (MUL). This study confirms MUL as a skeletal dysplasia with prenatal‐onset growth failure, slender bones, vertebral changes, and a high prevalence of fibrous dysplasia and fractures.
Susann Karlberg +3 more
wiley +1 more source
Effect of intranasal calcitonin in a patient with McCune-Albright Syndrome, fibrous dysplasia, and refractory bone pain [PDF]
McCune-Albright syndrome (MAS) is a rare disease defined by the triad of polyostotic fibrous dysplasia of bone, caf´e-au-lait skin spots, and precocious puberty. No available treatment is effective in changing the course of fibrous dysplasia of bone, but
Fighera, Tayane Muniz +1 more
core +5 more sources
Background: Fibrous dysplasia (FD) is a rare congenital bone disease. Denosumab, a monoclonal antibody targeting nuclear factor kappa‐B ligand (RANKL), suppresses osteoclast activity and exhibits therapeutic potential for FD. Case Presentation: We present the case of an adult female patient diagnosed with FD who had undergone 7 treatment cycles of ...
Danni Liu +5 more
wiley +1 more source
Background Cherubism is a rare genetic disorder characterised by multilocular cystic lesions in the mandible and/or maxilla, which result in the typical cherub‐like face. Two forms of cherubism exist—hereditary (familial) and nonhereditary (nonfamilial)—and it usually occurs amongst children aged 2–7 years.
Seth Kwadjo Angmorterh +11 more
wiley +1 more source
Fibrous Dysplasia: Clinicopathologic Presentation of 36 Cases
Objective: Fibrous dysplasia is a slowly progressing bone lesion resulting from displacement of the normal medullary bone with abnormal fibroosseous tissue.
Mine ÖZŞEN +3 more
doaj +1 more source
The nature of fibrous dysplasia [PDF]
Fibrous dysplasia has been regarded as a developmental skeletal disorder characterized by replacement of normal bone with benign cellular fibrous connective tissue.
A Corsi +24 more
core +3 more sources

