Results 171 to 180 of about 2,787 (193)
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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.
S, MEYERSOHN, I J, GREK
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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.
S, MEYERSOHN, I J, GREK
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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
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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
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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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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 ...
G E, Lello, O C, Sparrow
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Clinical Nuclear Medicine, 1984
Fibrous dysplasia, a bone dysplasia of unknown pathogenesis, may be either monostotic or polyostotic. Not only is the femur involved in nearly all cases of the polyostotic form, but a distinct unilateral predilection is often noted. The following case illustrates the classic polyostotic changes.
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Fibrous dysplasia, a bone dysplasia of unknown pathogenesis, may be either monostotic or polyostotic. Not only is the femur involved in nearly all cases of the polyostotic form, but a distinct unilateral predilection is often noted. The following case illustrates the classic polyostotic changes.
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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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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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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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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.
D. K. O’Donovan +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.
D. K. O’Donovan +3 more
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