Results 161 to 170 of about 144,018 (198)
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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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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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Polyostotic fibrous dysplasia of bone
Oral Surgery, Oral Medicine, Oral Pathology, 1958Present Illness.--The patient, a B-year-old white girl, was referred to this office by auother dentist on April 1, 1955, for removal of the upper and lower first and second deciduous molars, During the course of the examination, the entire clinical picture revealed itself (it will be presented in detail below).
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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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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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Polyostotic fibrous dysplasia with acromegaly
The American Journal of Medicine, 1985A 26-year-old man was found to have incomplete polyostotic fibrous dysplasia of bone and elevated growth hormone and prolactin levels. There was roentgenographic evidence of a pituitary tumor. The natural history of fibrous dysplasia in relationship to excess growth hormone secretion since childhood is described.
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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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Archives of Internal Medicine, 1939
The skeletal disease known as polyostotic fibrous dysplasia has been described in the literature under a variety of designations, including osteodystrophia fibrosa unilateralis, osteitis fibrosa localisata, osteodystrophia fibrosa cystica generalisata, fibrous osteodystrophy and osteitis fibrosa disseminata.
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The skeletal disease known as polyostotic fibrous dysplasia has been described in the literature under a variety of designations, including osteodystrophia fibrosa unilateralis, osteitis fibrosa localisata, osteodystrophia fibrosa cystica generalisata, fibrous osteodystrophy and osteitis fibrosa disseminata.
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