Results 71 to 80 of about 161,435 (256)
Monostotic Fibrous Dysplasia with Rare Histopathologic Features: A Case Report [PDF]
Iranian Journal of Medical SciencesFibrous dysplasia is a slow-progressing benign condition characterized by abnormal bone formation that leads to some skeletal disorders. Although some of the fibrous dysplasia have unusual clinical and radiographic features that can lead to a challenging
Abbas Karimi +5 more
doaj +1 more source
First two cases of craniomaxillofacial fibrous dysplasia from Nepal – case series
, 2018 Neha Mishra,1 Sourav Kumar Rout2 1Department of Oral and Maxillofacial Pathology and Microbiology, Chitwan Medical College and Teaching Hospital, Bharatpur-10, Chitwan, Nepal; 2Department of Oral and Maxillofacial Surgery, Chitwan Medical College and ...
Rout SK, Mishra N
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The Endothelial CXCR Family in Vascular Health and Disease
iNew Medicine, EarlyView.ABSTRACT Endothelial cells (ECs) form the dynamic interface between blood and tissue, serving as key regulators of vascular homeostasis, inflammation, and repair. Among the molecular systems governing endothelial behavior, the C‐X‐C motif chemokine receptor (CXCR) family—originally characterized in immunology for its roles in leukocyte trafficking and ...
Zhiming Wu +4 more
wiley +1 more source
Journal of Medical Case ReportsBackground Fibrous dysplasia is an uncommon bone disorder in which medullary bone is replaced by disorganized fibro-osseous tissue. Fibrous dysplasia typically exhibits slow growth that stabilizes with skeletal maturity.
Sujitra Tinnut +5 more
doaj +1 more source
A rare complication of craniofacial fibrous dysplasia
, 1998 Fibrous dysplasia is a rare disease, the cause of which in not entirely known. The most common clinical manifestations of fibrous dysplasia of the temporal bone are the presence of two different pathologic disorders: morphologic and functional.
CASCONE, PIERO +3 more
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Congenital short bowel syndrome: Clinical aspects by systematic review
JPGN Reports, EarlyView.Abstract Objectives Congenital short bowel syndrome (CSBS) is a rare intestinal disorder characterized by inborn shortening of the bowel with mainly mutations in Coxsackie and Adenovirus receptor‐like membrane protein (CLMP) and Filamin A (FLNA) genes.
Barblin Remund +2 more
wiley +1 more source
Journal of the Belgian Society of Radiology, 2013 Background: A 51-year-old male was referred to the hospital with pain on the right side of the thorax, without any apparent trauma. There was no medical history. He had a nonproductive cough and smoked 15 cigarettes a day. The patient did not have fever or weight loss and was not feeling ill. There was no history of asbestos contact.
Schouten, BJ, Suliman, HM
openaire +5 more sources
Fibrous dysplasia in a Monkey [PDF]
, 1962 Fibrous dysplasia is a syndrome characterized by dysplastic fibro-osseous skeletal changes. The syndrome has been described in the literature under a number of different terms including osteodystrophia fibrosa, polyostotic osteitis fibrosa, regional ...
Duncan, J. +3 more
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A Rare Case of Radiculopathy: Monostotic Fibrous Dysplasia of the Sacrum
Acta Médica Portuguesa, 2019 Fibrous dysplasia is a bone disease characterized by an osteoblastic dysfunction resulting in a fibrous replacement of the normal medullary bone. We describe the case of a 33-year-old who presented with low back pain irradiating to her right leg.
Joaquim Cruz Teixeira +3 more
doaj +1 more source
Craniofacial polyostotic fibrous dysplasia
, 2010 An unusual case of fibrous dysplasia involving right craniofacial region in a female is reported.
Chandan Prabhakar, Yadavalli Guruprasad
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