Results 151 to 160 of about 2,247 (190)
The hip in hereditary multiple exostoses
The Journal of Bone and Joint Surgery. British volume, 2001 We defined the characteristics of dysplasia and coxa valga in hereditary multiple exostoses (HME) by radiological analysis of 24 hips in 12 patients. The degree and effect of the ‘osteochondroma load’ around the hip were quantified. We investigated the pathology of the labrum and the incidence of osteoarthritis and of malignant change in these ...
D E, Porter, M K, Benson, G A, Hosney
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New England Journal of Medicine, 1949
HEREDITARY multiple exostoses are a distinct clinical entity more frequently encountered than is generally appreciated. We have recently had the opportunity of studying 4 members of a Negro family who had the condition. Few cases occurring in Negroes are reported in the American literature.1 2 3 To our knowledge this is the first Negro family studied ...
J, ROSE, P D, DOOLAN
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HEREDITARY multiple exostoses are a distinct clinical entity more frequently encountered than is generally appreciated. We have recently had the opportunity of studying 4 members of a Negro family who had the condition. Few cases occurring in Negroes are reported in the American literature.1 2 3 To our knowledge this is the first Negro family studied ...
J, ROSE, P D, DOOLAN
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Radiology, 1952
Hereditary multiple exostoses is a familial disturbance in the growth of cartilaginous bone tissue, most marked at the diaphyso-epiphyseal junction of the long bones. Until the report of Ehrenfried (1) in 1917, mention of this disease was relatively infrequent in the American literature, but since that time numerous cases have been reported (2).
J D, STARK, N N, ADLER, W H, ROBINSON
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Hereditary multiple exostoses is a familial disturbance in the growth of cartilaginous bone tissue, most marked at the diaphyso-epiphyseal junction of the long bones. Until the report of Ehrenfried (1) in 1917, mention of this disease was relatively infrequent in the American literature, but since that time numerous cases have been reported (2).
J D, STARK, N N, ADLER, W H, ROBINSON
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Hereditary Multiple Exostoses with Pseudoaneurysm
CardioVascular and Interventional Radiology, 2007A 16-year-old male patient with hereditary multiple exostoses (HME) was found to have a pseudoaneurysm of the left popliteal artery caused by osteochondroma in the lower femur. The diagnosis was confirmed by ultrasound, magnetic resonance imaging and magnetic resonance angiography without the need to perform an angiogram. The osteochondroma was excised
Azmy M, Al-Hadidy +5 more
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Manifestations of Hereditary Multiple Exostoses
Journal of the American Academy of Orthopaedic Surgeons, 2005The solitary osteochondroma, a common pediatric bone tumor, is a cartilage-capped exostosis. Hereditary multiple exostosis is an autosomal dominant disorder manifested by the presence of multiple osteochondromas. Linkage analysis has implicated mutations in the EXT gene family, resulting in an error in the regulation of normal chondrocyte proliferation
Jonathan R, Stieber, John P, Dormans
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Hereditary Multiple Exostoses With Myelopathy
Archives of Neurology, 1979A 58-year-old woman with hereditary multiple exostoses had slowly progressive myelopathy due to a vertebral exostosis that compressed the spinal cord at T1-2. She did not show skeletal deformities, but had numerous palpable long-bone exostoses. While CNS complications are rare in hereditary multiple exostosis, 17 other cases have been reported.
S U, Ho, H L, Lipton
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Hereditary multiple exostoses and enchondromatosis
Best Practice & Research Clinical Rheumatology, 2008Hereditary multiple exostoses (HME) is an autosomal-dominant disorder characterized by the development of benign tumours, multiple osteochondromas (exostoses), growing outward from the metaphyses of long bones. Birth prevalence is estimated to be one in 50,000, and the severity of the disease is variable.
Stéphanie, Pannier +1 more
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Clinical Orthopaedics and Related Research, 1984
In a family with hereditary multiple exostoses (diaphyseal aclasis), six generations are known to have been affected. Thirty-three of 85 family members have had the disorder. This condition affects the long bones, pelvis, scapulae, and ribs, and the exostoses continue to enlarge until epiphyseal fusion occurs.
B F, Crandall +3 more
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In a family with hereditary multiple exostoses (diaphyseal aclasis), six generations are known to have been affected. Thirty-three of 85 family members have had the disorder. This condition affects the long bones, pelvis, scapulae, and ribs, and the exostoses continue to enlarge until epiphyseal fusion occurs.
B F, Crandall +3 more
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Multiple hereditary exostoses and enchondromatosis
Best Practice & Research Clinical Rheumatology, 2020Multiple hereditary exostoses (MHE) and enchondromatosis are rare multifocal benign disorders usually causing skeletal deformities appearing already in childhood. MHE is a dominant autosomal inherited disorder characterized by multiple osteochondromas (exostoses) growing outward from the metaphyses of long bones as well as from flat bones.
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