Results 231 to 240 of about 11,914 (280)

Monostotic Fibrous Dysplasia with Rare Histopathologic Features: A Case Report. [PDF]

open access: yesIran J Med Sci
Karimi A   +5 more
europepmc   +1 more source

Polyostotic Fibrous Dysplasia

Proceedings of the Royal Society of Medicine, 1951
A case of polyostotic fibrous dysplasia in an African male is described. The case also had bilateral congenital cataracts and nerve deafness on the side affected by the dysplasia.
I. J. Grek, Sidney Meyersohn
openaire   +5 more sources

68Ga-PSMA-HBED-CC PET/CT Findings in a Patient of Polyostotic Fibrous Dysplasia.

Clinical Nuclear Medicine, 2021
A 43-year-old man diagnosed with fibrous dysplasia with McCune-Albright syndrome was subjected to 18F-fluoride bone scan and 68Ga-PSMA-HBED-CC PET/CT as per the institution protocol.
G. Malhotra   +3 more
semanticscholar   +1 more source

Polyostotic Fibrous Dysplasia With Extensive Cartilaginous Differentiation: A Rare Case Clinically Mimicking Ollier Disease

AJSP: Reviews and Reports, 2021
Fibrous dysplasia is a dysplastic disorder of bone caused by missense mutations of the GNAS1 gene. Fibrocartilaginous dysplasia (also known as fibrochondrodysplasia or fibrous dysplasia with extensive cartilaginous differentiation) is a rare variant of ...
Melanie H Hakar   +3 more
semanticscholar   +1 more source

Polyostotic Fibrous Dysplasia

Orthopedics, 2014
An 18-year-old man was referred to the authors’ institution’s thoracic cancer specialists for further consultation after abnormal findings were seen on chest radiograph.
Terrence C. Demos   +4 more
openaire   +3 more sources

Home - About - Disclaimer - Privacy