Results 201 to 210 of about 11,182 (240)
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Craniofacial polyostotic fibrous dysplasia
Journal of Maxillofacial Surgery, 1985Three cases of gross craniofacial polyostotic fibrous dysplasia are presented, together with a brief review of the condition, and pertinent points regarding the cases are discussed. As complete excision of the lesion and immediate reconstruction is rarely feasible or possible, and partial excision may result in accelerated growth of the lesion during ...
Owen C. Sparrow, Glenn E. Lello
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Irish Journal of Medical Science, 1944
A fairly typical example of polyostotic fibrous dysplasia is recorded in a girl of 4 1/2 years. There were some unusual features about the patient, such as retarded mental development, very extensive lesions in the bones, predominance of cartilage in bone biopsy and anaemia with nucleated red cells in the peripheral blood.
F. Duff +3 more
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A fairly typical example of polyostotic fibrous dysplasia is recorded in a girl of 4 1/2 years. There were some unusual features about the patient, such as retarded mental development, very extensive lesions in the bones, predominance of cartilage in bone biopsy and anaemia with nucleated red cells in the peripheral blood.
F. Duff +3 more
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Indian Journal of Otolaryngology, 1966
A case of fibrous dysplasia of polyostotic variety involving cervical spines, both sides of occipital bone besides mandible, maxilla, parietal, humerus, ulna, and radius of the left side is presented and briefly discussed.
Prem K. Kakar +2 more
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A case of fibrous dysplasia of polyostotic variety involving cervical spines, both sides of occipital bone besides mandible, maxilla, parietal, humerus, ulna, and radius of the left side is presented and briefly discussed.
Prem K. Kakar +2 more
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Familial polyostotic fibrous dysplasia
Oral Surgery, Oral Medicine, Oral Pathology, 1975A case of polyostotic fibrous dysplasia of the craniofacial type is presented, together with substantial evidence that this condition had a genetic basis in this patient. A review of the literature indicates that there is absolutely no previous evidence of a genetic basis to this condition.
M. Reitzik, J.F. Lownie
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The Journal of craniofacial surgery (Print), 2020
Fibrous dysplasia (FD) is a developmental bone disorder caused by the hamartamatous proliferation of bone-forming cells. A 29-year-old male patient with diagnosis of FD was admitted to our clinic with the symptoms of severe craniomaxillofacial ...
Kemalettin Yildiz +5 more
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Fibrous dysplasia (FD) is a developmental bone disorder caused by the hamartamatous proliferation of bone-forming cells. A 29-year-old male patient with diagnosis of FD was admitted to our clinic with the symptoms of severe craniomaxillofacial ...
Kemalettin Yildiz +5 more
semanticscholar +1 more source
The British Journal of Radiology, 1953
A case of polyostotic fibrous dysplasia in an African female is described. The case also had bilateral loss of smell sense and involvement of left paranasal sinuses, but no evidence of hormonal derangement or other changes in the skeleton.
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A case of polyostotic fibrous dysplasia in an African female is described. The case also had bilateral loss of smell sense and involvement of left paranasal sinuses, but no evidence of hormonal derangement or other changes in the skeleton.
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Extensive Polyostotic Craniofacial Fibrous Dysplasia With Optic Nerve Impingement.
The Journal of craniofacial surgery (Print), 2020Fibrous dysplasia is a benign overgrowth of metaplastic fibrous material resulting in disorganized deposition of bony matrix. Surgical intervention is the primary treatment modality.
Allison C. Hu +3 more
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Journal of the ASEAN Federation of Endocrine Societies
INTRODUCTION/BACKGROUNDFibrous Dysplasia is a rare developmental bone disorder in which fibro-osseous tissue replaces normal bone tissue. It can manifest either monostotic or polyostotic associated with McCune-Albright syndrome.
Jia Cheng Ong +2 more
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INTRODUCTION/BACKGROUNDFibrous Dysplasia is a rare developmental bone disorder in which fibro-osseous tissue replaces normal bone tissue. It can manifest either monostotic or polyostotic associated with McCune-Albright syndrome.
Jia Cheng Ong +2 more
semanticscholar +1 more source
Radiology, 1943
In the course of our examination of candidates for induction into the United States Army an example of a rather rare clinical syndrome was encountered. While this disease has been described in the literature under a variety of names, the one suggested by Lichtenstein (1)—polyostotic fibrous dysplasia—appears satisfactory and has been adopted in ...
Lewis E. Etter, John W. Hurst
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In the course of our examination of candidates for induction into the United States Army an example of a rather rare clinical syndrome was encountered. While this disease has been described in the literature under a variety of names, the one suggested by Lichtenstein (1)—polyostotic fibrous dysplasia—appears satisfactory and has been adopted in ...
Lewis E. Etter, John W. Hurst
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Polyostotic Fibrous Dysplasia in a Dog
Veterinary and Comparative Orthopaedics and Traumatology, 1998SummaryA young Dobermann Pincher dog with severe right hind leg lameness was admitted to our clinic. A complete radiographic examination showed the presence of cystic lesions in the right tibia and femur and polyostotic fibrous dysplasia was diagnosed.The distal tibial lesion, associated with an incomplete cortical fracture, was treated by surgical ...
DI MEO, Antonio +3 more
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